## Abstract We report the second case of a child with trisomy of the entire short arm of chromosome 17 secondary to a de novo duplication. Trisomy 17p in this patient resulted from a duplication, localized to the distal region of the long arm of the same chromosome, an abnormality not previously de
β¦ LIBER β¦
Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2
β Scribed by Areeg H. El-Gharbawy; Joseph N. Peeden Jr.; Ralph S. Lachman; John M. Graham Jr.; Stephen R. Moore; David L. Rimoin
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 185 KB
- Volume
- 152A
- Category
- Article
- ISSN
- 1552-4825
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