Intragenic rearrangements in X-linked intellectual deficiency: results of a-CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes. [electronic resource]
Producer: 20150331Description: 1991-7 p. digitalISSN:- 1552-4833
- Child, Preschool
- Chromosome Mapping
- Chromosomes, Human, X
- Comparative Genomic Hybridization
- DNA Copy Number Variations
- Gene Deletion
- Genes, X-Linked
- Genetic Loci
- Genome-Wide Association Study
- Humans
- Intellectual Disability -- diagnosis
- Male
- Microfilament Proteins -- genetics
- TRPC Cation Channels -- genetics
- Translocation, Genetic
- X Chromosome Inactivation
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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