Frequent detection of parental consanguinity in children with developmental disorders by a combined...
Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray
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Publisher
England: BioMed Central Ltd
Journal title
Language
English
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Publisher
England: BioMed Central Ltd
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Scope and Contents
Contents
Genomic microarrays have been used as the first-tier cytogenetic diagnostic test for patients with developmental delay/intellectual disability, autism spectrum disorders and/or multiple congenital anomalies. The use of SNP arrays has revealed regions of homozygosity in the genome which can lead to identification of uniparental disomy and parental c...
Alternative Titles
Full title
Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3853444
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3853444
Other Identifiers
ISSN
1755-8166
E-ISSN
1755-8166
DOI
10.1186/1755-8166-6-38
