Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: TBCE[original query] |
---|
Comprehensive next-generation sequencing analyses of hypoparathyroidism: identification of novel GCM2 mutations. The Journal of clinical endocrinology and metabolism 2014 Nov 99 (11): E2421-8. Mitsui Toshikatsu, Narumi Satoshi, Inokuchi Mikako, Nagasaki Keisuke, Nakazawa Mie, Sasaki Goro, Hasegawa Tomono |
Analysis of AP2S1, a calcium-sensing receptor regulator, in familial and sporadic isolated hypoparathyroidism. The Journal of clinical endocrinology and metabolism 2014 Mar 99 (3): E469-73. Lambert Anne-Sophie, Grybek Virginie, Francou Bruno, Esterle Laure, Bertrand Guylène, Bouligand Jérôme, Guiochon-Mantel Anne, Hieronimus Sylvie, Voitel Dorit, Soskin Sylvie, Magdelaine Corinne, Lienhardt Anne, Silve Caroline, Linglart Agn |
[A genomic study of adult-onset idiopathic hypoparathyroidism in Chinese by targeted next-generation sequencing]. Zhonghua nei ke za zhi 2016 Aug 55 (8): 604-8. Li Y P, Wang O, Quan T T, Xia W B, Jiang Y, Li M, Meng X W, Xing X |
A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness.
The Journal of clinical endocrinology and metabolism 2020 10 105 (10): . Dauber Andrew, Meng Yan, Audi Laura, Vedantam Sailaja, Weaver Benjamin, Carrascosa Antonio, Albertsson-Wikland Kerstin, Ranke Michael B, Jorge Alexander A L, Cara Jose, Wajnrajch Michael P, Lindberg Anders, Camacho-Hübner Cecilia, Hirschhorn Joel |
Disorders of Sex Development in a Large Ukrainian Cohort: Clinical Diversity and Genetic Findings. Frontiers in endocrinology 2022 4 13 810782. Globa Evgenia, Zelinska Natalia, Shcherbak Yulia, Bignon-Topalovic Joelle, Bashamboo Anu, M?Elreavey K |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: