Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23 (1991)
- Authors:
- USP affiliated authors: KOIFFMANN, CELIA PRISZKULNIK - IB ; WAJNTAL, ANITA - IB ; SOUZA, DEISE HELENA DE - IB ; GONZALEZ, CLAUDETTE HAJAJ - FM
- Unidades: IB; FM
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Source:
- Título do periódico: American Journal of Human Genetics
- Volume/Número/Paginação/Ano: v.49, n.4 suppl., p.243, oct. 1991
- Conference titles: International Congress of Human Genetics
-
ABNT
KOIFFMANN, Celia Priszkulnik et al. Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23. American Journal of Human Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 25 abr. 2024. , 1991 -
APA
Koiffmann, C. P., Gonzalez, C. H., Souza, D. H., Odone Filho, V., Kim, C. A., Moretti-Ferreira, D., & Wajntal, A. (1991). Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23. American Journal of Human Genetics. Instituto de Biociências, Universidade de São Paulo. -
NLM
Koiffmann CP, Gonzalez CH, Souza DH, Odone Filho V, Kim CA, Moretti-Ferreira D, Wajntal A. Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 243.[citado 2024 abr. 25 ] -
Vancouver
Koiffmann CP, Gonzalez CH, Souza DH, Odone Filho V, Kim CA, Moretti-Ferreira D, Wajntal A. Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 243.[citado 2024 abr. 25 ] - Shwachman syndrome (mckusick 26040): a chromosome breakage syndrome?
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- Cytogenetic evidence of involvement of chromosome regions 15q12 and 12q15 in conditions with associated overgrowth
- Dup (4) (q25_qter) mat e dup (4) (q31.3_qter) pat: estudo da variabilidade fenotipica na dup (4q)
- Microdelecao cromossomica na sindrome de cefalopolissindactilia de greig
- Chromosome abnormalities and tumors in syndromes leading to overgrowth
- Brief cytogenetic report on maternal translocation t(7; 9)(p22:p13): two sibs with duplication 9p and one sib with the balanced translocation
- Human situs determination and chromosome constitution 46, XY, ins(7;8)(q22;q12;q24). [Carta ao editor]
- Estudo genetico-clinico de sindromes associadas a regiao 15q11-13
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