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Article

Turner syndrome: the case of the missing sex chromosome.

Trends in genetics : TIG - 1 Mar 1993

Zinn A R, Page D C, Fisher E M

Abstract excerpt

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.

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Identifiers

PMID: 8488568
DOI: 10.1016/0168-9525(93)90230-f

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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