Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter. [electronic resource]
Producer: 20050810Description: 38-44 p. digitalISSN:- 1552-4825
- Abnormalities, Multiple -- genetics
- Adolescent
- Chromosome Deletion
- Chromosomes, Human, Pair 19 -- genetics
- Cleft Palate -- pathology
- Face -- abnormalities
- Genetic Predisposition to Disease -- genetics
- Hearing Loss -- pathology
- Heart Defects, Congenital -- pathology
- Humans
- Immune System -- abnormalities
- In Situ Hybridization, Fluorescence
- Keloid -- pathology
- Learning Disabilities -- pathology
- Male
- Phenotype
- Telomere -- genetics
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Publication Type: Case Reports; Journal Article; Review
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