11368137

Source:http://linkedlifedata.com/resource/pubmed/id/11368137

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0020028, umls-concept:C0022526, umls-concept:C0022885, umls-concept:C0033053, umls-concept:C0332464, umls-concept:C0392366, umls-concept:C0521457, umls-concept:C1158478, umls-concept:C1705422, umls-concept:C1710028
pubmed:issue	5
pubmed:dateCreated	2001-5-22
pubmed:abstractText	To investigate the applicability of carrier screening in women undergoing invasive prenatal diagnosis.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100935741
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	1470-0328
pubmed:author	pubmed-author:HeinonenSS, pubmed-author:KallinenJJ, pubmed-author:MannermaaAA, pubmed-author:MarinKK, pubmed-author:PalotieAA, pubmed-author:RyynänenMM
pubmed:issnType	Print
pubmed:volume	108
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	505-9
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:11368137-Cohort Studies, pubmed-meshheading:11368137-Female, pubmed-meshheading:11368137-Fragile X Syndrome, pubmed-meshheading:11368137-Genetic Testing, pubmed-meshheading:11368137-Heterozygote, pubmed-meshheading:11368137-Humans, pubmed-meshheading:11368137-Karyotyping, pubmed-meshheading:11368137-Lysosomal Storage Diseases, pubmed-meshheading:11368137-Neuronal Ceroid-Lipofuscinoses, pubmed-meshheading:11368137-Patient Acceptance of Health Care, pubmed-meshheading:11368137-Pregnancy, pubmed-meshheading:11368137-Prenatal Diagnosis, pubmed-meshheading:11368137-Prospective Studies
pubmed:year	2001
pubmed:articleTitle	Wide scope prenatal diagnosis at Kuopio University Hospital 1997-1998: integration of gene tests and fetal karyotyping.
pubmed:affiliation	Department of Obstetrics and Gynaecology, University Hospital of Kuopio, Finland.
pubmed:publicationType	Journal Article