Is routine karyotyping required in prenatal samples with a molecular or metabolic referral?
Is routine karyotyping required in prenatal samples with a molecular or metabolic referral?
About this item
Full title
Author / Creator
Publisher
England: BioMed Central
Journal title
Language
English
Formats
Publication information
Publisher
England: BioMed Central
Subjects
More information
Scope and Contents
Contents
As a routine, karyotyping of invasive prenatal samples is performed as an adjunct to referrals for DNA mutation detection and metabolic testing. We performed a retrospective study on 500 samples to assess the diagnostic value of this procedure. These samples included 454 (90.8%) chorionic villus (CV) and 46 (9.2%) amniocenteses specimens. For CV sa...
Alternative Titles
Full title
Is routine karyotyping required in prenatal samples with a molecular or metabolic referral?
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_29a5118450074e2390c91fed2a591cb9
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_29a5118450074e2390c91fed2a591cb9
Other Identifiers
ISSN
1755-8166
E-ISSN
1755-8166
DOI
10.1186/1755-8166-5-7
