Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortium
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics (clinical),General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s13023-019-1102-9.pdf
Reference91 articles.
1. Albright F, et al. Syndrome characterized by osteitis Fibrosa Disseminata, areas of pigmentation and endocrine dysfunction, with precocious puberty in females. N Engl J Med. 1937;216(17):727–46.
2. LIchenstein L. Polyostotic fibrous dysplasia. Arch Surg. 1938;36:874–8.
3. Weinstein LS, et al. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome. N Engl J Med. 1991;325(24):1688–95.
4. Landis CA, et al. GTPase inhibiting mutations activate the alpha chain of Gs and stimulate adenylyl cyclase in human pituitary tumours. Nature. 1989;340(6236):692–6.
5. Boyce AM, Collins MT. Fibrous Dysplasia/McCune-Albright Syndrome. In: Pagon RA, et al., editors. GeneReviews(R). Seattle: University of Washington; 1993. University of Washington, Seattle. All rights reserved.: Seattle (WA).
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