Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5 Pt 2
pubmed:dateCreated
2002-4-26
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.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0029-7844
pubmed:author
pubmed:issnType
Print
pubmed:volume
99
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
956-8
pubmed:dateRevised
2009-10-26
pubmed:meshHeading
pubmed:year
2002
pubmed:articleTitle
Abnormal first-trimester fetal nuchal translucency and Cornelia De Lange syndrome.
pubmed:affiliation
Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of California, California, Irvine, USA. wakamanmd@aol.com
pubmed:publicationType
Journal Article, Case Reports