Source:http://linkedlifedata.com/resource/pubmed/id/11975974
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5 Pt 2
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pubmed:dateCreated |
2002-4-26
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pubmed:abstractText |
Cornelia de Lange syndrome is a genetic disorder associated with delayed growth and characteristic facial features. There is no definitive biochemical or chromosomal marker for the prenatal diagnosis of this syndrome. We describe a case of Cornelia de Lange syndrome associated with an increased nuchal translucency in the first trimester.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0029-7844
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
99
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
956-8
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pubmed:dateRevised |
2009-10-26
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pubmed:meshHeading |
pubmed-meshheading:11975974-De Lange Syndrome,
pubmed-meshheading:11975974-Female,
pubmed-meshheading:11975974-Fetal Diseases,
pubmed-meshheading:11975974-Humans,
pubmed-meshheading:11975974-Neck,
pubmed-meshheading:11975974-Pregnancy,
pubmed-meshheading:11975974-Pregnancy Trimester, First,
pubmed-meshheading:11975974-Ultrasonography, Prenatal
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pubmed:year |
2002
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pubmed:articleTitle |
Abnormal first-trimester fetal nuchal translucency and Cornelia De Lange syndrome.
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pubmed:affiliation |
Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of California, California, Irvine, USA. wakamanmd@aol.com
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pubmed:publicationType |
Journal Article,
Case Reports
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