| Literature DB >> 8488568 |
A R Zinn1, D C Page, E M Fisher.
Abstract
Turner syndrome is the phenotype associated with the absence of a second sex chromosome in humans. Recent observations support the hypothesis that the phenotype results from haploid dosage of genes that are common to the X and Y chromosomes and that escape X inactivation. A goal of current studies is the identification of these "Turner' genes.Entities:
Mesh:
Year: 1993 PMID: 8488568 DOI: 10.1016/0168-9525(93)90230-f
Source DB: PubMed Journal: Trends Genet ISSN: 0168-9525 Impact factor: 11.639