|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
6
|
|
pubmed:dateCreated |
2000-1-7
|
|
pubmed:abstractText |
To value the rate of chromosomal abnormalities and evolution of children who had a prenatal diagnosis of fetal nuchal translucency in the first trimester.
|
|
pubmed:language |
fre
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Oct
|
|
pubmed:issn |
0368-2315
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
28
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
538-43
|
|
pubmed:dateRevised |
2007-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:10598347-Chromosome Aberrations,
pubmed-meshheading:10598347-Congenital Abnormalities,
pubmed-meshheading:10598347-Facial Bones,
pubmed-meshheading:10598347-Female,
pubmed-meshheading:10598347-Heart Defects, Congenital,
pubmed-meshheading:10598347-Humans,
pubmed-meshheading:10598347-Karyotyping,
pubmed-meshheading:10598347-Kidney,
pubmed-meshheading:10598347-Neck,
pubmed-meshheading:10598347-Pregnancy,
pubmed-meshheading:10598347-Prenatal Diagnosis,
pubmed-meshheading:10598347-Prospective Studies,
pubmed-meshheading:10598347-Trisomy,
pubmed-meshheading:10598347-Ultrasonography, Prenatal
|
|
pubmed:year |
1999
|
|
pubmed:articleTitle |
[Nuchal translucency: screening for chromosomal abnormalities and congenital malformations. Multicenter study].
|
|
pubmed:affiliation |
Maternité Jeanne de Flandre, Lille.
|
|
pubmed:publicationType |
Journal Article,
English Abstract
|
