Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)
- 1 March 2011
- journal article
- case report
- Published by Elsevier BV in Bone
- Vol. 48 (3), 659-662
- https://doi.org/10.1016/j.bone.2010.10.168
Abstract
No abstract availableKeywords
Funding Information
- National Institute of Diabetes and Digestive and Kidney Diseases (R01 DK073911, R37 DK46718)
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