FRAXA premutation associated with premature ovarian failure

FRAXA premutation associated with premature ovarian failure

Author ViannaMorgante, A. M. Google Scholar
Costa, S. S. Google Scholar
Pares, A. S. Google Scholar
Verreschi, ITN Google Scholar
Institution Universidade Federal de São Paulo (UNIFESP)
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. (C) 1996 Wiley-Liss, Inc.
Keywords premature ovarian failure
premature menopause
FRAXA premutation
FRAXA heterozygotes
Language English
Date 1996-08-09
Published in American Journal of Medical Genetics. New York: Wiley-liss, v. 64, n. 2, p. 373-375, 1996.
ISSN 0148-7299 (Sherpa/Romeo, impact factor)
Publisher Wiley-Blackwell
Extent 373-375
Origin http://dx.doi.org/10.1002/(SICI)1096-8628(19960809)64:2<373
Access rights Closed access
Type Article
Web of Science ID WOS:A1996VA12400029
URI http://repositorio.unifesp.br/handle/11600/25619

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