| Literature DB >> 8541840 |
S Barbaux1, E Vilain, O Raoul, S Gilgenkrantz, E Jeandidier, D Chadenas, N Souleyreau, M Fellous, K McElreavey.
Abstract
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 hypothesized that this specific phenotype was the consequence of the haploinsufficiency 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.Entities:
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Year: 1995 PMID: 8541840 DOI: 10.1093/hmg/4.9.1565
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150