Case Reports
doi: 10.1111/j.1442-200x.1990.tb00788.x.
Terminal deletion of chromosome 10q and its clinical features
Affiliations
- PMID: 2109493
- DOI: 10.1111/j.1442-200x.1990.tb00788.x
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Case Reports
Terminal deletion of chromosome 10q and its clinical features
Acta Paediatr Jpn.
1990 Feb.
Abstract
A male case with terminal deletion of chromosome 10q has growth retardation, craniofacial dysmorphism, congenital heart disease and other minor anomalies. The karyotypic formula is 46, XY, del (10), (q26.1----qter) by a high resolution G-banding staining. There are few differences in clinical features between our case and the previously reported cases.
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