Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray

BACKGROUND: 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 c...

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Detalles Bibliográficos
Autores principales: Fan, Yao-Shan, Ouyang, Xiaomei, Peng, Jinghong, Sacharow, Stephanie, Tekin, Mustafa, Barbouth, Deborah, Bodamer, Olaf, Yusupov, Roman, Navarrete, Christina, Heller, Ana H, Pena, Sérgio DJ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853444/
https://www.ncbi.nlm.nih.gov/pubmed/24053112
http://dx.doi.org/10.1186/1755-8166-6-38

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853444/
https://www.ncbi.nlm.nih.gov/pubmed/24053112
http://dx.doi.org/10.1186/1755-8166-6-38

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