Pseudohypoparathyroidism type I and Albright's hereditary osteodystrophy with a proximal 15q chromosomal deletion in mother and daughter
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03224.x/fullpdf
Reference40 articles.
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2. Studies on the attainment of normocalcemia in patients with pseudo-hypoparathyroidism;Breslau;Am J Med,1980
3. Prader-Willi syndrome: current understanding of cause and diagnosis;Butler;Am J Med Genet,1990
4. Prader-Willi syndrome;Cassidy;Neurol Clin,1989
5. Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome;Donlon;Proc Natl Acad Sci,1986
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