Interstitial 10p deletion derived from a maternal ins(16;10)(q22;p13p15.2): Report of the first familial case of 10p monosomy affecting to two familial members of different generations. [electronic resource]
Producer: 20170104Description: 1268-73 p. digitalISSN:- 1552-4833
- Adult
- Child
- Chromosome Deletion
- Chromosome Disorders -- genetics
- Chromosomes, Human, Pair 10 -- genetics
- Comparative Genomic Hybridization
- Developmental Disabilities -- genetics
- DiGeorge Syndrome -- genetics
- Gene Deletion
- Hearing Loss, Sensorineural -- genetics
- Humans
- Hypoparathyroidism -- genetics
- In Situ Hybridization, Fluorescence
- Karyotyping
- Male
- Nephrosis -- genetics
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Publication Type: Case Reports; Journal Article
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