FRAXA premutation associated with premature ovarian failure.
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.
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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