Molecular characterization of a patient with 3p deletion syndrome and a review of the literature. [electronic resource]
Producer: 20081209Description: 2746-52 p. digitalISSN:- 1552-4833
- Child, Preschool
- Chromosome Deletion
- Chromosome Disorders -- genetics
- Chromosomes, Human, Pair 13 -- genetics
- Chromosomes, Human, Pair 3 -- genetics
- Comparative Genomic Hybridization
- Craniofacial Abnormalities -- genetics
- Developmental Disabilities -- genetics
- Female
- Humans
- In Situ Hybridization, Fluorescence
- Karyotyping
- Limb Deformities, Congenital -- genetics
- Male
- Phenotype
- Syndrome
- Translocation, Genetic
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
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