Autor:	A M, Vianna-Morgante, S S, Costa, A S, Pares, I T, Verreschi
Rok vydání:	1996
Předmět:	Adult Male Heterozygote X Chromosome Adolescent Fragile X Syndrome Mutation Humans Female DNA Primary Ovarian Insufficiency Pedigree
Zdroj:	American journal of medical genetics. 64(2)
ISSN:	0148-7299
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::f80e845c74e4a12218e64b31a3055a09 https://pubmed.ncbi.nlm.nih.gov/8844084 Zobrazit plný text záznamu Plný text