Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant? [electronic resource]
Producer: 20100714Description: 93-9 p. digitalISSN:- 1878-0849
- Abnormalities, Multiple -- genetics
- Adolescent
- Autistic Disorder -- genetics
- Child
- Child, Preschool
- Chromosomes, Human, X -- genetics
- Cohort Studies
- Comparative Genomic Hybridization
- Female
- Gene Dosage
- Gene Duplication
- Genetic Variation
- Genetics, Behavioral
- Humans
- Infant
- Infant, Newborn
- Intellectual Disability -- genetics
- Male
- Phenotype
- Polymorphism, Single Nucleotide
- Steryl-Sulfatase -- genetics
- X Chromosome Inactivation
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Publication Type: Journal Article
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