PROXIMAL DELETIONS OF THE LONG ARM OF THE Y-CHROMOSOME SUGGEST A CRITICAL REGION ASSOCIATED WITH A SPECIFIC SUBSET OF CHARACTERISTIC TURNER STIGMATA

被引:17
作者
BARBAUX, S
VILAIN, E
RAOUL, O
GILGENKRANTZ, S
JEANDIDIER, E
CHADENAS, D
SOULEYREAU, N
FELLOUS, M
MCELREAVEY, K
机构
[1] HOP NECKER ENFANTS MALAD,SERV HISTOL EMBRYOL & CYTOGENET,F-75015 PARIS,FRANCE
[2] CTR REG TRANSFUS & HEMATOL,CYTOGENET LAB,F-54511 VANDOEUVRE NANCY,FRANCE
[3] CTR HOSP ORLEANS,CYTOGENET LAB,F-68051 MULHOUSE,FRANCE
[4] HOP SOURCE ORLEANS,CTR HOSP,F-45067 ORLEANS 2,FRANCE
关键词
D O I
10.1093/hmg/4.9.1565
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Turner syndrome is a complex human disorder that generally associates a 45,X karyotype to a female phenotype presenting with gonadal dysgenesis, short stature and a number of characteristic somatic features. It has been hypothesised that this specific phenotype was the consequence of the hapolinsufficiency of some X-linked genes having functional homologs on the Y chromosome. Here we describe four patients with deletions of the long arm of their Y chromosome and presenting with azoospermia and with or without Turner stigmata. Analysis of their breakpoints by Southern blotting and Y-specific sequence tagged sites (STS) allows us to delimit a region located in proximal interval 5 of the Y chromosome involved in skeletal development and growth.
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收藏
页码:1565 / 1568
页数:4
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