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Artigo de periodico
Waardenburg syndrome: clinical differentiation between types I and II (2003)
Pardono, Eliete; Bever, Yolande van; Ende, Jenneke van den; Havrenne, Poti Chimetta; Iughetti, Paula; Maestrelli, Sylvia Regina Pedrosa; Costa Filho, Orozimbo Alves; Richieri-Costa, Antonio; Frota-Pessoa, Oswaldo; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidades: FOB, HRAC, IB
Assunto: ANORMALIDADES CRANIOFACIAIS
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ABNT
PARDONO, Eliete et al. Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, v. 117A, n. 3, p. 223-235, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10193. Acesso em: 19 abr. 2024.
APA
Pardono, E., Bever, Y. van, Ende, J. van den, Havrenne, P. C., Iughetti, P., Maestrelli, S. R. P., et al. (2003). Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, 117A( 3), 223-235. doi:10.1002/ajmg.a.10193
NLM
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Vancouver
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Artigo de periodico
Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report] (1985)
Richieri-Costa, Antonio; Coletto, G M D D; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA
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ABNT
RICHIERI-COSTA, Antonio e COLETTO, G M D D e OTTO, Paulo A. Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report]. American Journal of Medical Genetics, v. 21, n. 4, p. 637-642, 1985Tradução . . Acesso em: 19 abr. 2024.
APA
Richieri-Costa, A., Coletto, G. M. D. D., & Otto, P. A. (1985). Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report]. American Journal of Medical Genetics, 21( 4), 637-642.
NLM
Richieri-Costa A, Coletto GMDD, Otto PA. Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report]. American Journal of Medical Genetics. 1985 ; 21( 4): 637-642.[citado 2024 abr. 19 ]
Vancouver
Richieri-Costa A, Coletto GMDD, Otto PA. Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report]. American Journal of Medical Genetics. 1985 ; 21( 4): 637-642.[citado 2024 abr. 19 ]
Artigo de periodico-carta/editorial
Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial] (1999)
Vianna-Morgante, Angela M
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
VIANNA-MORGANTE, Angela M. Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 1999
APA
Vianna-Morgante, A. M. (1999). Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Vianna-Morgante AM. Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. 1999 ; 83( 4): 326.[citado 2024 abr. 19 ]
Vancouver
Vianna-Morgante AM. Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. 1999 ; 83( 4): 326.[citado 2024 abr. 19 ]
Artigo de periodico
Treatment of duchenne muscular dystrophy with growth hormone inhibitors (1986)
Zatz, Mayana ; Betti, R T B; Frota-Pessoa, O
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR (TRATAMENTO), DOENÇAS GENÉTICAS, GENÉTICA, HORMÔNIOS
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ABNT
ZATZ, Mayana e BETTI, R T B e FROTA-PESSOA, O. Treatment of duchenne muscular dystrophy with growth hormone inhibitors. American Journal of Medical Genetics, v. 24, p. 549-66, 1986Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320240322. Acesso em: 19 abr. 2024.
APA
Zatz, M., Betti, R. T. B., & Frota-Pessoa, O. (1986). Treatment of duchenne muscular dystrophy with growth hormone inhibitors. American Journal of Medical Genetics, 24, 549-66. doi:10.1002/ajmg.1320240322
NLM
Zatz M, Betti RTB, Frota-Pessoa O. Treatment of duchenne muscular dystrophy with growth hormone inhibitors [Internet]. American Journal of Medical Genetics. 1986 ;24 549-66.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320240322
Vancouver
Zatz M, Betti RTB, Frota-Pessoa O. Treatment of duchenne muscular dystrophy with growth hormone inhibitors [Internet]. American Journal of Medical Genetics. 1986 ;24 549-66.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320240322
Artigo de periodico-carta/editorial
Transposon-like element in the dystrophin gene. [Carta ao editor] (1993)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Vainzof, Mariz
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: DISTROFIA MUSCULAR
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ABNT
ZATZ, Mayana e PASSOS-BUENO, Maria Rita e VAINZOF, Mariz. Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 1993
APA
Zatz, M., Passos-Bueno, M. R., & Vainzof, M. (1993). Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Passos-Bueno MR, Vainzof M. Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. 1993 ; 46( 5): 601.[citado 2024 abr. 19 ]
Vancouver
Zatz M, Passos-Bueno MR, Vainzof M. Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. 1993 ; 46( 5): 601.[citado 2024 abr. 19 ]
Artigo de periodico
The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome (1980)
Otto, Paulo A ; Otto, Priscila Guimarães
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: SÍNDROME DE DOWN
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ABNT
OTTO, Paulo A e OTTO, Priscila Guimarães. The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome. American Journal of Medical Genetics, v. 6, p. 145-152, 1980Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320060208. Acesso em: 19 abr. 2024.
APA
Otto, P. A., & Otto, P. G. (1980). The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome. American Journal of Medical Genetics, 6, 145-152. doi:10.1002/ajmg.1320060208
NLM
Otto PA, Otto PG. The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome [Internet]. American Journal of Medical Genetics. 1980 ; 6 145-152.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320060208
Vancouver
Otto PA, Otto PG. The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome [Internet]. American Journal of Medical Genetics. 1980 ; 6 145-152.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320060208
Artigo de periodico
Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis (1998)
Rabbi-Bortolini, Eliete; Bernardino, Andréa L F; Lopes, Adoris L; Ferri, Adriana da Silva; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
RABBI-BORTOLINI, Eliete et al. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis. American Journal of Medical Genetics, v. 76, p. 288-290, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q. Acesso em: 19 abr. 2024.
APA
Rabbi-Bortolini, E., Bernardino, A. L. F., Lopes, A. L., Ferri, A. da S., Passos-Bueno, M. R., & Zatz, M. (1998). Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis. American Journal of Medical Genetics, 76, 288-290. doi:10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q
NLM
Rabbi-Bortolini E, Bernardino ALF, Lopes AL, Ferri A da S, Passos-Bueno MR, Zatz M. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis [Internet]. American Journal of Medical Genetics. 1998 ; 76 288-290.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q
Vancouver
Rabbi-Bortolini E, Bernardino ALF, Lopes AL, Ferri A da S, Passos-Bueno MR, Zatz M. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis [Internet]. American Journal of Medical Genetics. 1998 ; 76 288-290.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q
Artigo de periodico
Social adjustment in adult males affected with progressive muscular dystrophy (1998)
Eggers, Sabine; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
EGGERS, Sabine e ZATZ, Mayana. Social adjustment in adult males affected with progressive muscular dystrophy. American Journal of Medical Genetics, v. 81, p. 4-12, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980207)81:1%3C4::aid-ajmg2%3E3.0.co;2-#. Acesso em: 19 abr. 2024.
APA
Eggers, S., & Zatz, M. (1998). Social adjustment in adult males affected with progressive muscular dystrophy. American Journal of Medical Genetics, 81, 4-12. doi:10.1002/(sici)1096-8628(19980207)81:1%3C4::aid-ajmg2%3E3.0.co;2-#
NLM
Eggers S, Zatz M. Social adjustment in adult males affected with progressive muscular dystrophy [Internet]. American Journal of Medical Genetics. 1998 ; 81 4-12.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980207)81:1%3C4::aid-ajmg2%3E3.0.co;2-#
Vancouver
Eggers S, Zatz M. Social adjustment in adult males affected with progressive muscular dystrophy [Internet]. American Journal of Medical Genetics. 1998 ; 81 4-12.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980207)81:1%3C4::aid-ajmg2%3E3.0.co;2-#
Artigo de periodico
Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? (1993)
Passos-Bueno, Maria Rita ; Byth, B C; Rosemberg, Sérgio; Takata, R I; Bakker, E; Beggs, A H; Pavanello, R C M; Vainzof, Mariz ; Davies, K E; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidades: FM, IB
Assunto: GENÉTICA MÉDICA
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ABNT
PASSOS-BUENO, Maria Rita et al. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation?. American Journal of Medical Genetics, v. 46, n. 2 , p. 172-5, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460214. Acesso em: 19 abr. 2024.
APA
Passos-Bueno, M. R., Byth, B. C., Rosemberg, S., Takata, R. I., Bakker, E., Beggs, A. H., et al. (1993). Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? American Journal of Medical Genetics, 46( 2 ), 172-5. doi:10.1002/ajmg.1320460214
NLM
Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320460214
Vancouver
Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320460214
Artigo de periodico
Severe Nonspecific X-Linked Mental Retardation Caused by a-Proximally Xp Located Gene: intragenic Heterogeneity or a New Form of X-Linked Mental Retardation? (1993)
Passos-Bueno, Maria Rita ; Byth, Barbara C; Rosenberg, Sergio; Takata, Reinaldo I; Bakker, Egbert ; Beggs, Alan H ; Pavanello, Rita C; Vainzof, Mariz ; Davies, Kay E; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: RETARDO MENTAL, HETEROGENEIDADE, CROMOSSOMO X
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ABNT
PASSOS-BUENO, Maria Rita et al. Severe Nonspecific X-Linked Mental Retardation Caused by a-Proximally Xp Located Gene: intragenic Heterogeneity or a New Form of X-Linked Mental Retardation?. American Journal of Medical Genetics, v. 46, p. 172-175, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460214. Acesso em: 19 abr. 2024.
APA
Passos-Bueno, M. R., Byth, B. C., Rosenberg, S., Takata, R. I., Bakker, E., Beggs, A. H., et al. (1993). Severe Nonspecific X-Linked Mental Retardation Caused by a-Proximally Xp Located Gene: intragenic Heterogeneity or a New Form of X-Linked Mental Retardation? American Journal of Medical Genetics, 46, 172-175. doi:10.1002/ajmg.1320460214
NLM
Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, Vainzof M, Davies KE, Zatz M. Severe Nonspecific X-Linked Mental Retardation Caused by a-Proximally Xp Located Gene: intragenic Heterogeneity or a New Form of X-Linked Mental Retardation? [Internet]. American Journal of Medical Genetics. 1993 ; 46 172-175.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320460214
Vancouver
Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, Vainzof M, Davies KE, Zatz M. Severe Nonspecific X-Linked Mental Retardation Caused by a-Proximally Xp Located Gene: intragenic Heterogeneity or a New Form of X-Linked Mental Retardation? [Internet]. American Journal of Medical Genetics. 1993 ; 46 172-175.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320460214
Artigo de periodico
Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G (1999)
Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Moreira, Eloisa S.; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G. American Journal of Medical Genetics, v. 82, p. 392-398, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0. Acesso em: 19 abr. 2024.
APA
Passos-Bueno, M. R., Vainzof, M., Moreira, E. S., & Zatz, M. (1999). Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G. American Journal of Medical Genetics, 82, 392-398. doi:10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
NLM
Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G [Internet]. American Journal of Medical Genetics. 1999 ; 82 392-398.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
Vancouver
Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G [Internet]. American Journal of Medical Genetics. 1999 ; 82 392-398.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
Artigo de periodico
Serum ck-mb activity in progressive muscular dystrophy: is it of nosologic value? (1985)
Vainzof, Mariz ; Zatz, Mayana ; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES
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ABNT
VAINZOF, Mariz e ZATZ, Mayana e OTTO, Paulo A. Serum ck-mb activity in progressive muscular dystrophy: is it of nosologic value?. American Journal of Medical Genetics, v. 22, p. 81-7, 1985Tradução . . Acesso em: 19 abr. 2024.
APA
Vainzof, M., Zatz, M., & Otto, P. A. (1985). Serum ck-mb activity in progressive muscular dystrophy: is it of nosologic value? American Journal of Medical Genetics, 22, 81-7.
NLM
Vainzof M, Zatz M, Otto PA. Serum ck-mb activity in progressive muscular dystrophy: is it of nosologic value? American Journal of Medical Genetics. 1985 ;22 81-7.[citado 2024 abr. 19 ]
Vancouver
Vainzof M, Zatz M, Otto PA. Serum ck-mb activity in progressive muscular dystrophy: is it of nosologic value? American Journal of Medical Genetics. 1985 ;22 81-7.[citado 2024 abr. 19 ]
Artigo de periodico
Serum b-glucuronidase enxyme activity in progressive muscular dystrophies: a preliminary study (1985)
Vainzof, Mariz ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DOENÇAS NEUROMUSCULARES, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz e ZATZ, Mayana. Serum b-glucuronidase enxyme activity in progressive muscular dystrophies: a preliminary study. American Journal of Medical Genetics, v. 21, p. 395-8, 1985Tradução . . Acesso em: 19 abr. 2024.
APA
Vainzof, M., & Zatz, M. (1985). Serum b-glucuronidase enxyme activity in progressive muscular dystrophies: a preliminary study. American Journal of Medical Genetics, 21, 395-8.
NLM
Vainzof M, Zatz M. Serum b-glucuronidase enxyme activity in progressive muscular dystrophies: a preliminary study. American Journal of Medical Genetics. 1985 ;21 395-8.[citado 2024 abr. 19 ]
Vancouver
Vainzof M, Zatz M. Serum b-glucuronidase enxyme activity in progressive muscular dystrophies: a preliminary study. American Journal of Medical Genetics. 1985 ;21 395-8.[citado 2024 abr. 19 ]
Artigo de periodico-carta/editorial
Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta] (1999)
Pereira, Lygia da Veiga ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Lygia da Veiga e ZATZ, Mayana. Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 1999
APA
Pereira, L. da V., & Zatz, M. (1999). Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Pereira L da V, Zatz M. Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. 1999 ; 87 86-87.[citado 2024 abr. 19 ]
Vancouver
Pereira L da V, Zatz M. Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. 1999 ; 87 86-87.[citado 2024 abr. 19 ]
Artigo de periodico
Screening of male patients with autosomal recessive duchenne dystrophy through dystrophin and dna studies (1991)
Vainzof, Mariz ; Pavanello, R C M; Pavanello Filho, I; Rapaport, D; Passos-Bueno, Maria Rita ; Zubrzycka-Gaarn, E E; Bulman, D E; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Screening of male patients with autosomal recessive duchenne dystrophy through dystrophin and dna studies. American Journal of Medical Genetics, v. 39, p. 38-41, 1991Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320390110. Acesso em: 19 abr. 2024.
APA
Vainzof, M., Pavanello, R. C. M., Pavanello Filho, I., Rapaport, D., Passos-Bueno, M. R., Zubrzycka-Gaarn, E. E., et al. (1991). Screening of male patients with autosomal recessive duchenne dystrophy through dystrophin and dna studies. American Journal of Medical Genetics, 39, 38-41. doi:10.1002/ajmg.1320390110
NLM
Vainzof M, Pavanello RCM, Pavanello Filho I, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Bulman DE, Zatz M. Screening of male patients with autosomal recessive duchenne dystrophy through dystrophin and dna studies [Internet]. American Journal of Medical Genetics. 1991 ;39 38-41.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320390110
Vancouver
Vainzof M, Pavanello RCM, Pavanello Filho I, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Bulman DE, Zatz M. Screening of male patients with autosomal recessive duchenne dystrophy through dystrophin and dna studies [Internet]. American Journal of Medical Genetics. 1991 ;39 38-41.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320390110
Artigo de periodico
Schinzel–Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 and literature review of the clinical features (2015)
Carvalho, Ellaine; Honjo, Rachel; Magalhães, Monize; Yamamoto, Guilherme; Rocha, Katia; Naslavsky, Michel ; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Kim, Chong
Source: American Journal of Medical Genetics. Unidades: IB, FM
Subjects: GENÉTICA MÉDICA, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA
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ABNT
CARVALHO, Ellaine et al. Schinzel–Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 and literature review of the clinical features. American Journal of Medical Genetics, p. on-line., 2015Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36789. Acesso em: 19 abr. 2024.
APA
Carvalho, E., Honjo, R., Magalhães, M., Yamamoto, G., Rocha, K., Naslavsky, M., et al. (2015). Schinzel–Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 and literature review of the clinical features. American Journal of Medical Genetics, on-line. doi:10.1002/ajmg.a.36789
NLM
Carvalho E, Honjo R, Magalhães M, Yamamoto G, Rocha K, Naslavsky M, Zatz M, Passos-Bueno MR, Kim C. Schinzel–Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 and literature review of the clinical features [Internet]. American Journal of Medical Genetics. 2015 ; on-line.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.36789
Vancouver
Carvalho E, Honjo R, Magalhães M, Yamamoto G, Rocha K, Naslavsky M, Zatz M, Passos-Bueno MR, Kim C. Schinzel–Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 and literature review of the clinical features [Internet]. American Journal of Medical Genetics. 2015 ; on-line.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.36789
Artigo de periodico-carta/editorial
Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta] (1999)
Gaspar, D A; Pavanello, R.C; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Andre, M; Steman, S; Wyszynski, D. F; Matioli, Sergio Russo
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, LÁBIO FISSURADO, MUTAÇÃO GENÉTICA, POLIMORFISMO, MALFORMAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GASPAR, D A et al. Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta]. American Journal of Medical Genetics. Hoboken: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.CO;2-M. Acesso em: 19 abr. 2024. , 1999
APA
Gaspar, D. A., Pavanello, R. C., Zatz, M., Passos-Bueno, M. R., Andre, M., Steman, S., et al. (1999). Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta]. American Journal of Medical Genetics. Hoboken: Instituto de Biociências, Universidade de São Paulo. doi:10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.
NLM
Gaspar DA, Pavanello RC, Zatz M, Passos-Bueno MR, Andre M, Steman S, Wyszynski DF, Matioli SR. Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta] [Internet]. American Journal of Medical Genetics. 1999 ; 87 197-199.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.CO;2-M
Vancouver
Gaspar DA, Pavanello RC, Zatz M, Passos-Bueno MR, Andre M, Steman S, Wyszynski DF, Matioli SR. Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta] [Internet]. American Journal of Medical Genetics. 1999 ; 87 197-199.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.CO;2-M
Artigo de periodico-carta/editorial
Response to Dr. Meisner. [Carta ao editor] (1990)
Mingroni Netto, Regina Celia ; Rosenberg, Carla ; Vianna-Morgante, Angela M ; Pavanello, Rita de Cássia M.
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: RETARDO MENTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia et al. Response to Dr. Meisner. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 1990
APA
Mingroni Netto, R. C., Rosenberg, C., Vianna-Morgante, A. M., & Pavanello, R. de C. M. (1990). Response to Dr. Meisner. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Mingroni Netto RC, Rosenberg C, Vianna-Morgante AM, Pavanello R de CM. Response to Dr. Meisner. [Carta ao editor]. American Journal of Medical Genetics. 1990 ; 37 434.[citado 2024 abr. 19 ]
Vancouver
Mingroni Netto RC, Rosenberg C, Vianna-Morgante AM, Pavanello R de CM. Response to Dr. Meisner. [Carta ao editor]. American Journal of Medical Genetics. 1990 ; 37 434.[citado 2024 abr. 19 ]
Artigo de periodico
Relationship of expansion of cgg repeats and x-inactivation with expression of fra (x) (q27.3) in heterozygotes (1994)
Mingroni Netto, Regina Celia ; Fernandes, J G; Vianna-Morgante, Angela M
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia e FERNANDES, J G e VIANNA-MORGANTE, Angela M. Relationship of expansion of cgg repeats and x-inactivation with expression of fra (x) (q27.3) in heterozygotes. American Journal of Medical Genetics, v. 51, n. 4 , p. 443-6, 1994Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320510427. Acesso em: 19 abr. 2024.
APA
Mingroni Netto, R. C., Fernandes, J. G., & Vianna-Morgante, A. M. (1994). Relationship of expansion of cgg repeats and x-inactivation with expression of fra (x) (q27.3) in heterozygotes. American Journal of Medical Genetics, 51( 4 ), 443-6. doi:10.1002/ajmg.1320510427
NLM
Mingroni Netto RC, Fernandes JG, Vianna-Morgante AM. Relationship of expansion of cgg repeats and x-inactivation with expression of fra (x) (q27.3) in heterozygotes [Internet]. American Journal of Medical Genetics. 1994 ;51( 4 ): 443-6.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320510427
Vancouver
Mingroni Netto RC, Fernandes JG, Vianna-Morgante AM. Relationship of expansion of cgg repeats and x-inactivation with expression of fra (x) (q27.3) in heterozygotes [Internet]. American Journal of Medical Genetics. 1994 ;51( 4 ): 443-6.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320510427
Artigo de periodico
Relationship between mayer-rokitansky-kuster (mrk) anomaly and hereditary renal adysplasia (hra) (1988)
Pavanello, R C M; Eigier, A; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAVANELLO, R C M e EIGIER, A e OTTO, Paulo A. Relationship between mayer-rokitansky-kuster (mrk) anomaly and hereditary renal adysplasia (hra). American Journal of Medical Genetics, v. 29, n. 4 , p. 845-9, 1988Tradução . . Acesso em: 19 abr. 2024.
APA
Pavanello, R. C. M., Eigier, A., & Otto, P. A. (1988). Relationship between mayer-rokitansky-kuster (mrk) anomaly and hereditary renal adysplasia (hra). American Journal of Medical Genetics, 29( 4 ), 845-9.
NLM
Pavanello RCM, Eigier A, Otto PA. Relationship between mayer-rokitansky-kuster (mrk) anomaly and hereditary renal adysplasia (hra). American Journal of Medical Genetics. 1988 ;29( 4 ): 845-9.[citado 2024 abr. 19 ]
Vancouver
Pavanello RCM, Eigier A, Otto PA. Relationship between mayer-rokitansky-kuster (mrk) anomaly and hereditary renal adysplasia (hra). American Journal of Medical Genetics. 1988 ;29( 4 ): 845-9.[citado 2024 abr. 19 ]

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