Turner syndrome: the case of the missing sex chromosome
Identifieur interne : 00CD07 ( Main/Exploration ); précédent : 00CD06; suivant : 00CD08Turner syndrome: the case of the missing sex chromosome
Auteurs : Andrew R. Zinn [États-Unis] ; David C. Page [États-Unis] ; Elizabeth M. C. Fisher [Royaume-Uni]Source :
- Trends in Genetics [ 0168-9525 ] ; 1993.
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.
Url:
DOI: 10.1016/0168-9525(93)90230-F
Affiliations:
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Zinn</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><wicri:regionArea>Howard Hughes Research Laboratories at the Whitehead Institute, and in The Department of Biology, Massachusetts Institute of Technology, Cambridge Center, Cambridge, MA 02142</wicri:regionArea><placeName><region type="state">Massachusetts</region></placeName></affiliation></author><author><name sortKey="Page, David C" sort="Page, David C" uniqKey="Page D" first="David C." last="Page">David C. Page</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><wicri:regionArea>Howard Hughes Research Laboratories at the Whitehead Institute, and in The Department of Biology, Massachusetts Institute of Technology, Cambridge Center, Cambridge, MA 02142</wicri:regionArea><placeName><region type="state">Massachusetts</region></placeName></affiliation></author><author><name sortKey="Fisher, Elizabeth M C" sort="Fisher, Elizabeth M C" uniqKey="Fisher E" first="Elizabeth M. C." last="Fisher">Elizabeth M. C. Fisher</name><affiliation wicri:level="3"><country>Royaume-Uni</country><wicri:regionArea>Department of Biochemistry and Molecular Genetics, St Mary's Hospital Medical School, Norfolix Place, London</wicri:regionArea><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j">Trends in Genetics</title><title level="j" type="abbrev">TIGS</title><idno type="ISSN">0168-9525</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1993">1993</date><biblScope unit="volume">9</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="90">90</biblScope><biblScope unit="page" to="93">93</biblScope></imprint><idno type="ISSN">0168-9525</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0168-9525</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">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.</div></front></TEI><affiliations><list><country><li>Royaume-Uni</li><li>États-Unis</li></country><region><li>Angleterre</li><li>Grand Londres</li><li>Massachusetts</li></region><settlement><li>Londres</li></settlement></list><tree><country name="États-Unis"><region name="Massachusetts"><name sortKey="Zinn, Andrew R" sort="Zinn, Andrew R" uniqKey="Zinn A" first="Andrew R." last="Zinn">Andrew R. Zinn</name></region><name sortKey="Page, David C" sort="Page, David C" uniqKey="Page D" first="David C." last="Page">David C. Page</name></country><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Fisher, Elizabeth M C" sort="Fisher, Elizabeth M C" uniqKey="Fisher E" first="Elizabeth M. C." last="Fisher">Elizabeth M. C. 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