2004
DOI: 10.1016/j.mce.2004.05.002
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Screening of FSH receptor gene in Argentine women with premature ovarian failure (POF)

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Cited by 48 publications
(38 citation statements)
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“…Other reports from American, German, Brazilian, Mexican and Argentine population [11,12,15,16,30] showed absence of this FSHR gene mutation in the subjects studied. However, Jiang et al, in 1998 [31], identified only one mutation (C 566 T) carrier in large scale screening of 1,162 subjects from Switzerland.…”
Section: Discussionmentioning
confidence: 53%
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“…Other reports from American, German, Brazilian, Mexican and Argentine population [11,12,15,16,30] showed absence of this FSHR gene mutation in the subjects studied. However, Jiang et al, in 1998 [31], identified only one mutation (C 566 T) carrier in large scale screening of 1,162 subjects from Switzerland.…”
Section: Discussionmentioning
confidence: 53%
“…We believe that the C 1723 T transition is a mutation because it was detected in only one case out of the total 236 subjects recruited; controls (n =100), subjects with amenorrhea (n=86) and subjects undergoing Assisted Reproductive Technology programme, having normal cyclicity (n=50; unpublished data), by RFLP analysis and DNA sequencing. This novel mutation has not been reported earlier in any of the studies so far [3,11,14,16,36].…”
Section: Hormonementioning
confidence: 54%
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“…Em 2004, Sundblad e cols. descreveram os resultados do rastreamento do gene do FSHR em mulheres argentinas com FOP, não tendo encontrado nenhuma com mutação, porém vinte delas apresentavam os polimorfismos Ala307Thr e Ser680Ans (33).…”
Section: Alterações Relacionadas a Genes Autossômicosunclassified