Human situs determination and chromosome constitution 46, XY, ins(7;8)(q22;q12;q24). [Carta ao editor] (1993)
- Authors:
- USP affiliated authors: KOIFFMANN, CELIA PRISZKULNIK - IB ; WAJNTAL, ANITA - IB ; GONZALEZ, CLAUDETTE HAJAJ - FM
- Unidades: IB; FM
- Assunto: CROMOSSOMOS
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics
- ISSN: 0148-7299
- Volume/Número/Paginação/Ano: v. 47, n. 4, p. 568-569, 1993
-
ABNT
KOIFFMANN, Celia Priszkulnik et al. Human situs determination and chromosome constitution 46, XY, ins(7;8)(q22;q12;q24). [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 04 ago. 2025. , 1993 -
APA
Koiffmann, C. P., Wajntal, A., Souza, D. H. de, Gonzalez, C. H., & Coates, M. V. (1993). Human situs determination and chromosome constitution 46, XY, ins(7;8)(q22;q12;q24). [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. -
NLM
Koiffmann CP, Wajntal A, Souza DH de, Gonzalez CH, Coates MV. Human situs determination and chromosome constitution 46, XY, ins(7;8)(q22;q12;q24). [Carta ao editor]. American Journal of Medical Genetics. 1993 ; 47( 4): 568-569.[citado 2025 ago. 04 ] -
Vancouver
Koiffmann CP, Wajntal A, Souza DH de, Gonzalez CH, Coates MV. Human situs determination and chromosome constitution 46, XY, ins(7;8)(q22;q12;q24). [Carta ao editor]. American Journal of Medical Genetics. 1993 ; 47( 4): 568-569.[citado 2025 ago. 04 ] - Brief cytogenetic report on maternal translocation t(7; 9)(p22:p13): two sibs with duplication 9p and one sib with the balanced translocation
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- História natural de 24 pacientes com trissomia 18 (síndrome de Edwards) e de 20 pacientes com trissomia 13 (síndrome de Patau)
- Shwachman syndrome (mckusick 26040): a chromosome breakage syndrome?
- Is shwachman syndrome (mckusick 26040) a chromosome breakage syndrome?
- Congenital scalp skull defects with distal limb anomalies (Adams-Oliver Syndrome - Mckusick 100030): further suggestion of autosomal recessive inheritance
- Estudo genético-clínico de 20 pacientes com trissomia 13(síndrome de Patau)
- Sindrome do triplo x: relato de 3 casos
- Sindrome do triplo x: relato de 4 casos
- Estudo genético-clínico de 24 pacientes com trissomia 18 (síndrome de Edwards)
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