Chromosome abnormalities and tumors in syndromes leading to overgrowth (1991)
- Authors:
- USP affiliated authors: KOIFFMANN, CELIA PRISZKULNIK - IB ; WAJNTAL, ANITA - IB ; SOUZA, DEISE HELENA DE - IB
- Unidade: IB
- Assunto: GENÉTICA ANIMAL
- Language: Inglês
- Imprenta:
- Publisher: Short Reports
- Publisher place: Miami
- Date published: 1991
- Source:
- Título: Proceedings
- Conference titles: Miami Bio-Technology Winter Symposium on Advances in Gene Technology: the Molecular Biology of Human Genetic Disease
-
ABNT
WAJNTAL, Anita et al. Chromosome abnormalities and tumors in syndromes leading to overgrowth. 1991, Anais.. Miami: Short Reports, 1991. . Acesso em: 03 out. 2024. -
APA
Wajntal, A., Koiffmann, C. P., Souza, D. H., & Moretti-Ferreira, D. (1991). Chromosome abnormalities and tumors in syndromes leading to overgrowth. In Proceedings. Miami: Short Reports. -
NLM
Wajntal A, Koiffmann CP, Souza DH, Moretti-Ferreira D. Chromosome abnormalities and tumors in syndromes leading to overgrowth. Proceedings. 1991 ;[citado 2024 out. 03 ] -
Vancouver
Wajntal A, Koiffmann CP, Souza DH, Moretti-Ferreira D. Chromosome abnormalities and tumors in syndromes leading to overgrowth. Proceedings. 1991 ;[citado 2024 out. 03 ] - Cytogenetic evidence of involvement of chromosome regions 15q12 and 12q15 in conditions with associated overgrowth
- Macrocephaly , multiple lipomas , and hemangiomata (bannayan-zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms?
- Shwachman syndrome (mckusick 26040): a chromosome breakage syndrome?
- Ring chromosome 7 in a man with multiple congenital anomalies and mental retardation
- Is shwachman syndrome (mckusick 26040) a chromosome breakage syndrome?
- Microcefalia , desaceleração pos-natal do crescimento, facies peculiar e deficiencia mental
- Constituicao cromossomica rara - 47, XXX/48, XXXX - em mulher normal
- Incontinentia pigmenti achromians (hipomelanose de ito) mim 146150 ; translocacao x / autossomo, sugerindo provavel localizacao do gene em xp11 para uma das formas dessa anomalia, muito heterogenea
- Microcefalia , desaceleração pós-natal do crescimento, faceis peculiar e deficiencia mental
- Sindrome disruptiva possivelmente causada por hipertermia materna
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