Cutaneous and Superficial Soft Tissue Lesions Associated With Albright Hereditary Osteodystrophy: Clinicopathological and Molecular Genetic Study of 4 Cases, Including a Novel Mutation of the GNAS Gene-Reference-Cited by-同舟云学术

Cutaneous and Superficial Soft Tissue Lesions Associated With Albright Hereditary Osteodystrophy: Clinicopathological and Molecular Genetic Study of 4 Cases, Including a Novel Mutation of the GNAS Gene

Published:2008-10 Issue:5 Volume:30 Page:417-424
ISSN:0193-1091
Container-title:The American Journal of Dermatopathology
language:en
Short-container-title:

Author:

Kacerovska Denisa,Nemcova Jana,Pomahacova Renata,Michal Michal,Kazakov Dmitry V

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Dermatology,General Medicine,Pathology and Forensic Medicine

Reference40 articles.

1. Pseudohypoparathyroidism-an example of Seabright-bantam syndrome: report of three cases.;Albright;Endocrinology,1942

2. Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism.;De Sanctis;Pediatr Res,2003

3. Albrights hereditary osteodystrophy and pseudohypoparathyroidism.;Wilson;Semin Musculoskelet Radiol,2002

4. GNAS locus and pseudohypoparathyroidism.;Bastepe;Horm Res,2005

5. Albrights hereditary osteodystrophy (pseudohypoparathyroidism type Ia): clinical case with a novel mutation of GNAS1.;Garavelli;Acta Biomed,2005

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