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Artigo de periodico
Cerebrofaciothoracic syndrome (1996)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio; Saavedra, Dolores; Cohen Junior, M. Michael
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine et al. Cerebrofaciothoracic syndrome. American Journal of Medical Genetics, v. 61, n. Ja 1996, p. 152-153, 1996Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C152::aid-ajmg9%3E3.0.co;2-z. Acesso em: 27 abr. 2024.
APA
Guion-Almeida, M. L., Richieri-Costa, A., Saavedra, D., & Cohen Junior, M. M. (1996). Cerebrofaciothoracic syndrome. American Journal of Medical Genetics, 61( Ja 1996), 152-153. doi:10.1002/(sici)1096-8628(19960111)61:2%3C152::aid-ajmg9%3E3.0.co;2-z
NLM
Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen Junior MM. Cerebrofaciothoracic syndrome [Internet]. American Journal of Medical Genetics. 1996 ; 61( Ja 1996): 152-153.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C152::aid-ajmg9%3E3.0.co;2-z
Vancouver
Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen Junior MM. Cerebrofaciothoracic syndrome [Internet]. American Journal of Medical Genetics. 1996 ; 61( Ja 1996): 152-153.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C152::aid-ajmg9%3E3.0.co;2-z
Artigo de periodico
Frontonasal dysplasia: analysis of 21 cases and literature review (1996)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio; Saavedra, Dolores; Cohen Junior, M. Michael
Source: International Journal of Maxillofacial Surgery. Unidade: HRAC
Subjects: SÍNDROMES OROFACIODIGITAIS, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine et al. Frontonasal dysplasia: analysis of 21 cases and literature review. International Journal of Maxillofacial Surgery, v. 25, n. 2, p. 91-97, 1996Tradução . . Disponível em: https://doi.org/10.1016/s0901-5027(96)80048-8. Acesso em: 27 abr. 2024.
APA
Guion-Almeida, M. L., Richieri-Costa, A., Saavedra, D., & Cohen Junior, M. M. (1996). Frontonasal dysplasia: analysis of 21 cases and literature review. International Journal of Maxillofacial Surgery, 25( 2), 91-97. doi:10.1016/s0901-5027(96)80048-8
NLM
Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen Junior MM. Frontonasal dysplasia: analysis of 21 cases and literature review [Internet]. International Journal of Maxillofacial Surgery. 1996 ; 25( 2): 91-97.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/s0901-5027(96)80048-8
Vancouver
Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen Junior MM. Frontonasal dysplasia: analysis of 21 cases and literature review [Internet]. International Journal of Maxillofacial Surgery. 1996 ; 25( 2): 91-97.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/s0901-5027(96)80048-8
Artigo de periodico
Craniofrontonasal syndrome: study of 41 patients (1996)
Saavedra, Dolores; Richieri-Costa, Antonio; Guion-Almeida, Maria Leine; Cohen Junior, M. Michael
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SAAVEDRA, Dolores et al. Craniofrontonasal syndrome: study of 41 patients. American Journal of Medical Genetics, v. 61, n. Ja 1996, p. 147-151, 1996Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C147::aid-ajmg8%3E3.0.co;2-u. Acesso em: 27 abr. 2024.
APA
Saavedra, D., Richieri-Costa, A., Guion-Almeida, M. L., & Cohen Junior, M. M. (1996). Craniofrontonasal syndrome: study of 41 patients. American Journal of Medical Genetics, 61( Ja 1996), 147-151. doi:10.1002/(sici)1096-8628(19960111)61:2%3C147::aid-ajmg8%3E3.0.co;2-u
NLM
Saavedra D, Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Craniofrontonasal syndrome: study of 41 patients [Internet]. American Journal of Medical Genetics. 1996 ; 61( Ja 1996): 147-151.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C147::aid-ajmg8%3E3.0.co;2-u
Vancouver
Saavedra D, Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Craniofrontonasal syndrome: study of 41 patients [Internet]. American Journal of Medical Genetics. 1996 ; 61( Ja 1996): 147-151.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C147::aid-ajmg8%3E3.0.co;2-u
Artigo de periodico
Hypertelorism: interobital growth, measurements, and pathogenetic considerations (1995)
Cohen Junior, M. Michael; Richieri-Costa, A; Guion-Almeida, Maria Leine; Saavedra, Dolores
Source: International Journal of Oral Maxillofacial Surgery. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COHEN JUNIOR, M. Michael et al. Hypertelorism: interobital growth, measurements, and pathogenetic considerations. International Journal of Oral Maxillofacial Surgery, v. 24, p. 387-395, 1995Tradução . . Disponível em: https://doi.org/10.1016/s0901-5027(05)80465-5. Acesso em: 27 abr. 2024.
APA
Cohen Junior, M. M., Richieri-Costa, A., Guion-Almeida, M. L., & Saavedra, D. (1995). Hypertelorism: interobital growth, measurements, and pathogenetic considerations. International Journal of Oral Maxillofacial Surgery, 24, 387-395. doi:10.1016/s0901-5027(05)80465-5
NLM
Cohen Junior MM, Richieri-Costa A, Guion-Almeida ML, Saavedra D. Hypertelorism: interobital growth, measurements, and pathogenetic considerations [Internet]. International Journal of Oral Maxillofacial Surgery. 1995 ;24 387-395.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/s0901-5027(05)80465-5
Vancouver
Cohen Junior MM, Richieri-Costa A, Guion-Almeida ML, Saavedra D. Hypertelorism: interobital growth, measurements, and pathogenetic considerations [Internet]. International Journal of Oral Maxillofacial Surgery. 1995 ;24 387-395.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/s0901-5027(05)80465-5
Artigo de periodico
Newly recognized autosomal recessive MCA/MR/overgrowth syndrome (1993)
Richieri-Costa, Antonio; Guion-Almeida, Maria Leine; Cohen Junior, M. Michael
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e GUION-ALMEIDA, Maria Leine e COHEN JUNIOR, M. Michael. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics, v. 47, n. 2, p. 278-280, 1993Tradução . . Acesso em: 27 abr. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., & Cohen Junior, M. M. (1993). Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics, 47( 2), 278-280.
NLM
Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics. 1993 ; 47( 2): 278-280.[citado 2024 abr. 27 ]
Vancouver
Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics. 1993 ; 47( 2): 278-280.[citado 2024 abr. 27 ]
Artigo de periodico
Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents (1993)
Richieri-Costa, Antonio; Pirolo Junior, L; Cohen Junior, M. Michael
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e PIROLO JUNIOR, L e COHEN JUNIOR, M. Michael. Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents. American Journal of Medical Genetics, v. 47, n. 2, p. 281-283, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320470228. Acesso em: 27 abr. 2024.
APA
Richieri-Costa, A., Pirolo Junior, L., & Cohen Junior, M. M. (1993). Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents. American Journal of Medical Genetics, 47( 2), 281-283. doi:10.1002/ajmg.1320470228
NLM
Richieri-Costa A, Pirolo Junior L, Cohen Junior MM. Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents [Internet]. American Journal of Medical Genetics. 1993 ; 47( 2): 281-283.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.1320470228
Vancouver
Richieri-Costa A, Pirolo Junior L, Cohen Junior MM. Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents [Internet]. American Journal of Medical Genetics. 1993 ; 47( 2): 281-283.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.1320470228
Artigo de periodico
Newly recognized blepharofacioskeletal syndrome (1993)
Richieri-Costa, Antonio; Guion-Almeida, Maria Leine; Rodini, Elaine Sbroggio de Oliveira; Pereira, S C D; Cohen Junior, M. Michael
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio et al. Newly recognized blepharofacioskeletal syndrome. American Journal of Medical Genetics, v. 46, n. 6, p. 620-622, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460603. Acesso em: 27 abr. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., Rodini, E. S. de O., Pereira, S. C. D., & Cohen Junior, M. M. (1993). Newly recognized blepharofacioskeletal syndrome. American Journal of Medical Genetics, 46( 6), 620-622. doi:10.1002/ajmg.1320460603
NLM
Richieri-Costa A, Guion-Almeida ML, Rodini ES de O, Pereira SCD, Cohen Junior MM. Newly recognized blepharofacioskeletal syndrome [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 620-622.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.1320460603
Vancouver
Richieri-Costa A, Guion-Almeida ML, Rodini ES de O, Pereira SCD, Cohen Junior MM. Newly recognized blepharofacioskeletal syndrome [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 620-622.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.1320460603

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