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Turner syndrome and haploinsufficiency

Identifieur interne : 000168 ( Istex/Corpus ); précédent : 000167; suivant : 000169

Turner syndrome and haploinsufficiency

Auteurs : Andrew R. Zinn ; Judith L. Ross

Source :

Current Opinion in Genetics & Development [ 0959-437X ] ; 1998.

RBID : ISTEX:03836DA9A352B16DF09FB0AE189FE74963B9B8D1

Abstract

Turner syndrome was one of the first human genetic disorders ascribed to haploinsufficiency but the identification of specific genes responsible for the phenotype has been problematic. Recent data point to several candidate genes, some new and some old, for specific aspects of the phenotype associated with monosomy X in humans.

Url:

https://api.istex.fr/document/03836DA9A352B16DF09FB0AE189FE74963B9B8D1/fulltext/pdf

DOI: 10.1016/S0959-437X(98)80089-0

Links to Exploration step

ISTEX:03836DA9A352B16DF09FB0AE189FE74963B9B8D1

Le document en format XML

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Turner syndrome and haploinsufficiency

Turner syndrome and haploinsufficiency

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Abstract

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