FRAXA premutation associated with premature ovarian failure

dc.contributorUniversidade Federal de São Paulo (UNIFESP)
dc.creatorVianna-Morgante, Angela M.
dc.creatorCosta, Silvia S.
dc.creatorPares, Annunziata Sonia Fusaro da Silva [UNIFESP]
dc.creatorVerreschi, Ieda Therezinha do Nascimento [UNIFESP]
dc.date.accessioned2016-01-24T11:40:34Z
dc.date.available2016-01-24T11:40:34Z
dc.date.created2016-01-24T11:40:34Z
dc.date.issued1996-08-09
dc.identifierAmerican Journal of Medical Genetics. New York: Wiley-liss, v. 64, n. 2, p. 373-375, 1996.
dc.identifier0148-7299
dc.identifierhttps://repositorio.unifesp.br/handle/11600/25619
dc.identifier10.1002/(SICI)1096-8628(19960809)64:2<373
dc.identifierWOS:A1996VA12400029
dc.description.abstractA 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.
dc.languageeng
dc.publisherWiley-Blackwell
dc.relationAmerican Journal of Medical Genetics
dc.rightshttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dc.rightsAcesso restrito
dc.subjectPremature ovarian failure
dc.subjectPremature menopause
dc.subjectFRAXA premutation
dc.subjectFRAXA heterozygotes
dc.titleFRAXA premutation associated with premature ovarian failure
dc.typeArtigo


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