Artigo
FRAXA premutation associated with premature ovarian failure
Fecha
1996-08-09Registro en:
American Journal of Medical Genetics. New York: Wiley-liss, v. 64, n. 2, p. 373-375, 1996.
0148-7299
10.1002/(SICI)1096-8628(19960809)64:2<373
WOS:A1996VA12400029
Autor
Vianna-Morgante, Angela M.
Costa, Silvia S.
Pares, Annunziata Sonia Fusaro da Silva [UNIFESP]
Verreschi, Ieda Therezinha do Nascimento [UNIFESP]
Institución
Resumen
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. (C) 1996 Wiley-Liss, Inc.