Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability. [electronic resource]
Producer: 20170424Description: e0175962 p. digitalISSN:- 1932-6203
- Antigens, Neoplasm -- genetics
- Child
- Child, Preschool
- Chromosomal Proteins, Non-Histone -- genetics
- Chromosome Duplication -- genetics
- Chromosomes, Human, X -- genetics
- Comparative Genomic Hybridization -- methods
- Developmental Disabilities -- genetics
- Female
- Genes, X-Linked -- genetics
- Humans
- Intellectual Disability -- genetics
- Male
- Neoplasm Proteins -- genetics
- Pedigree
- Peptide Termination Factors -- genetics
- Phenotype
- Sequence Deletion -- genetics
- X Chromosome Inactivation -- genetics
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Publication Type: Journal Article
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