Premature ovarian failure (POF) in brazilian fragile X carriers (1997)
- Authors:
- USP affiliated authors: MORGANTE, ANGELA MARIA VIANNA - IB ; OTTO, PAULO ALBERTO - IB ; MINGRONI NETTO, REGINA CELIA - IB
- Unidade: IB
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts POF-2
- Conference titles: International Workshop on Fragile X and X-Linked Mental Retardation
-
ABNT
VIANNA-MORGANTE, Angela M et al. Premature ovarian failure (POF) in brazilian fragile X carriers. 1997, Anais.. Picton: Instituto de Biociências, Universidade de São Paulo, 1997. . Acesso em: 31 dez. 2025. -
APA
Vianna-Morgante, A. M., Costa, S. C., Otto, P. A., & Mingroni Netto, R. C. (1997). Premature ovarian failure (POF) in brazilian fragile X carriers. In Abstracts POF-2. Picton: Instituto de Biociências, Universidade de São Paulo. -
NLM
Vianna-Morgante AM, Costa SC, Otto PA, Mingroni Netto RC. Premature ovarian failure (POF) in brazilian fragile X carriers. Abstracts POF-2. 1997 ;[citado 2025 dez. 31 ] -
Vancouver
Vianna-Morgante AM, Costa SC, Otto PA, Mingroni Netto RC. Premature ovarian failure (POF) in brazilian fragile X carriers. Abstracts POF-2. 1997 ;[citado 2025 dez. 31 ] - X-inactivation in fragile-X carriers
- Princípios de genética humana e médica
- Heterogeneidade genetica na ectrodactilia
- Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families
- Ectrodactilia associada à hemimelia tibial não segrega com marcadores dos cromossomos 7 e 10
- Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data
- Chromosome imbalances in syndromic hearing loss
- Distribution of CGG repeats and GRAXAC1/DXS548 alleles in south american populations
- Increased frequency of gray zone-premutated fraxa alleles in brazilian mentally impaired boys
- Origin of fmr-1 mutation: study of closely linked microsatellite loci in fragile x syndrome
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