Turner syndrome and haploinsufficiency

Andrew R. Zinn; Judith L. Ross

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

Turner syndrome and haploinsufficiency

Andrew R. Zinn, Judith L. Ross

Research output: Contribution to journal › Article › peer-review

104 Scopus citations

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.

Original language	English (US)
Pages (from-to)	322-327
Number of pages	6
Journal	Current Opinion in Genetics and Development
Volume	8
Issue number	3
DOIs	https://doi.org/10.1016/S0959-437X(98)80089-0
State	Published - Jun 1998

ASJC Scopus subject areas

Genetics
Developmental Biology

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title = "Turner syndrome and haploinsufficiency",

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.",

author = "Zinn, {Andrew R.} and Ross, {Judith L.}",

note = "Funding Information: The authors are supported by a grant from the National Institutes of Health (NS35554-01).",

year = "1998",

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AU - Ross, Judith L.

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N2 - 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.

AB - 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.

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Turner syndrome and haploinsufficiency

Abstract

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