Severe growth retardation, delayed bone age, and facial dysmorphism in two patients with microduplications in 2p16 → p22. [electronic resource]
Producer: 20140702Description: 3176-81 p. digitalISSN:- 1552-4833
- Basic Helix-Loop-Helix Transcription Factors -- genetics
- Child
- Chromosome Duplication -- genetics
- Chromosomes, Human, Pair 2 -- genetics
- Comparative Genomic Hybridization
- Developmental Disabilities -- genetics
- Female
- Humans
- Intellectual Disability -- genetics
- Male
- rho GTP-Binding Proteins -- genetics
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Publication Type: Case Reports; Journal Article
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