20p11 deletion in a female child with panhypopituitarism, cleft lip and palate, dysmorphic facial features, global developmental delay and seizure disorder. [electronic resource]
Producer: 20110517Description: 186-91 p. digitalISSN:- 1552-4833
- Abnormalities, Multiple -- genetics
- Brain -- pathology
- Chromosome Aberrations
- Chromosomes, Human, Pair 20 -- genetics
- Comparative Genomic Hybridization
- Developmental Disabilities -- genetics
- Female
- Humans
- Hypopituitarism -- genetics
- In Situ Hybridization, Fluorescence
- Infant
- Magnetic Resonance Imaging
- Microarray Analysis
- Phenotype
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Publication Type: Case Reports; Journal Article
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