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FRAXA premutation associated with premature ovarian failure.
Vianna-Morgante, A M; Costa, S S; Pares, A S; Verreschi, I T.
Afiliación
  • Vianna-Morgante AM; Departamento de Biologia, Universidade de São Paulo, Brazil.
Am J Med Genet ; 64(2): 373-5, 1996 Aug 09.
Article en En | MEDLINE | ID: mdl-8844084
ABSTRACT
A family is described in which six females in three generations experienced premature ovarian failure (POF). In three of them a FRAXA premutation was documented and the carrier status of a fourth female could be inferred, because her son had the fragile X syndrome. These findings provide further evidence for a nonrandom association between POF and the FRAXA premutation.
Asunto(s)
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Banco de datos: MEDLINE Asunto principal: Insuficiencia Ovárica Primaria / Síndrome del Cromosoma X Frágil / Heterocigoto / Mutación Tipo de estudio: Risk_factors_studies Límite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Am J Med Genet Año: 1996 Tipo del documento: Article País de afiliación: Brasil
Buscar en Google
Banco de datos: MEDLINE Asunto principal: Insuficiencia Ovárica Primaria / Síndrome del Cromosoma X Frágil / Heterocigoto / Mutación Tipo de estudio: Risk_factors_studies Límite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Am J Med Genet Año: 1996 Tipo del documento: Article País de afiliación: Brasil