Albright Hereditary Osteodystrophy
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-62345-6_5213
Reference9 articles.
1. Albright, F., Burnett, C. H., Smith, P. H., & Parson, W. (1942). Pseudohypoparathyroidism – An example ‘Seabright-Bantam syndrome’. Endocrinology, 30, 922–932.
2. Davies, S. J., & Hughes, H. E. (1993). Imprinting in Albright’s hereditary osteodystrophy. Journal of Medical Genetics, 30, 101–103.
3. de Nanclares, G. P., Fernández-Rebollo, E., Santin, I., García-Cuartero, B., et al. (2007). Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright’s hereditary osteodystrophy. The Journal of Clinical Endocrinology and Metabolism, 92(6), 2370–2373.
4. Kacerovska, D., Nemcova, J., Pomahacova, R., Michal, M., & Kazakov, D. V. (2008). 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. The American Journal of Dermatopathology, 30(5), 417–424.
5. Long, D. N., McGuire, S., Levine, M. A., Weinstein, L. S., & Germain-Lee, E. L. (2007). Body mass index differences in Pseudohypoparathyroidism type 1a versus Pseudo-pseudohypoparathyroidism may implicate paternal imprinting of Galpha(s) in the development of human obesity. The Journal of Clinical Endocrinology and Metabolism, 92, 1073–1079.
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