Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism?jaw tumour syndrome-Reference-Cited by-同舟云学术

Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism?jaw tumour syndrome

Published:2006-07 Issue:1 Volume:65 Page:9-16
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Mizusawa Noriko,Uchino Shinya,Iwata Takeo,Tsuyuguchi Masaru,Suzuki Yasuyo,Mizukoshi Tsunenori,Yamashita Yoshio,Sakurai Akihiro,Suzuki Shinichi,Beniko Mutsuo,Tahara Hideki,Fujisawa Masato,Kamata Nobuyuki,Fujisawa Kenji,Yashiro Tohru,Nagao Daisuke,Golam Hossain Md.,Sano Toshiaki,Noguchi Shiro,Yoshimoto Katsuhiko

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2006.02534.x/fullpdf

Reference37 articles.

1. Molecular genetics of multiple endocrine neoplasia types 1 and 2

2. Extracellular Calcium Sensing and Extracellular Calcium Signaling

3. Familial Isolated Hyperparathyroidism

4. Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome

5. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome

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