Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies. [electronic resource]
Producer: 20030407Description: 207-12 p. digitalISSN:- 0148-7299
- Abnormalities, Multiple -- genetics
- Chromosome Deletion
- Chromosome Mapping
- Chromosomes, Human, Pair 10 -- genetics
- Craniofacial Abnormalities -- pathology
- Developmental Disabilities -- pathology
- DiGeorge Syndrome -- genetics
- Heart Defects, Congenital -- pathology
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Male
- Microsatellite Repeats
- Syndactyly -- pathology
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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