A del(13)(q21.32q31.2)dn refined to 21.9 Mb in a female toddler with irides heterochromia and hypopigmentation: appraisal of interstitial mid-13q deletions. [electronic resource]
Producer: 20170206Description: 33-37 p. digitalISSN:- 1473-5717
- Brain -- pathology
- Child
- Child, Preschool
- Chromosome Banding
- Chromosome Deletion
- Chromosomes, Human, Pair 13
- Comparative Genomic Hybridization
- Female
- Genetic Association Studies
- Humans
- Hypopigmentation -- diagnosis
- Iris Diseases -- diagnosis
- Magnetic Resonance Imaging
- Phenotype
- Pigmentation Disorders -- diagnosis
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Publication Type: Case Reports; Journal Article
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