rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
7539
|
pubmed:dateCreated |
2006-2-24
|
pubmed:abstractText |
To investigate an approach for the analysis of samples obtained in screening for trisomy 21 that retains the advantages of quantitative fluorescent polymerase chain reaction (qf-PCR) over full karyotyping and maximises the detection of clinically significant abnormalities.
|
pubmed:commentsCorrections |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
1468-5833
|
pubmed:author |
|
pubmed:issnType |
Electronic
|
pubmed:day |
25
|
pubmed:volume |
332
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
452-5
|
pubmed:dateRevised |
2009-11-18
|
pubmed:meshHeading |
pubmed-meshheading:16476673-Adolescent,
pubmed-meshheading:16476673-Adult,
pubmed-meshheading:16476673-Aneuploidy,
pubmed-meshheading:16476673-Female,
pubmed-meshheading:16476673-Humans,
pubmed-meshheading:16476673-Karyotyping,
pubmed-meshheading:16476673-Middle Aged,
pubmed-meshheading:16476673-Nuchal Translucency Measurement,
pubmed-meshheading:16476673-Polymerase Chain Reaction,
pubmed-meshheading:16476673-Pregnancy,
pubmed-meshheading:16476673-Pregnancy, High-Risk,
pubmed-meshheading:16476673-Pregnancy Trimester, First,
pubmed-meshheading:16476673-Prenatal Diagnosis
|
pubmed:year |
2006
|
pubmed:articleTitle |
Fetal nuchal translucency scan and early prenatal diagnosis of chromosomal abnormalities by rapid aneuploidy screening: observational study.
|
pubmed:affiliation |
Clinical and Molecular Genetics, Institute of Child Health and UCLH, London WC1N 1EH.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|