Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Syndrome and GATA3[original query] |
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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 |
Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome. Scientific reports 2015 5 9511. Liao Dan, Hou Shengping, Zhang Jun, Fang Jing, Liu Yunjia, Bai Lin, Cao Qingfeng, Kijlstra Aize, Yang Peize |
From Genetic Predisposition to Molecular Mechanisms of Autoimmune Primary Adrenal Insufficiency. Frontiers of hormone research 2016 46 115-32. Falorni Alberto, Brozzetti Annalisa, Perniola Rober |
Philadelphia Chromosome-like Acute Lymphoblastic Leukemia. Clinical lymphoma, myeloma & leukemia 2017 8 17 (8): 464-470. Pui Ching-Hon, Roberts Kathryn G, Yang Jun J, Mullighan Charles |
Targeted Next-Generation Sequencing of 406 Genes Identified Genetic Defects Underlying Congenital Heart Disease in Down Syndrome Patients. Pediatric cardiology 2018 Aug . Alharbi Khalid M, Al-Mazroea Abdelhadi H, Abdallah Atiyeh M, Almohammadi Yousef, Carlus S Justin, Basit Sulm |
Genetic Screening in a Large Chinese Cohort of Childhood Onset Hypoparathyroidism by Next-Generation Sequencing Combined with TBX1-MLPA. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2019 8 34 (12): 2254-2263. Wang Yabing, Nie Min, Wang Ou, Li Yuepeng, Jiang Yan, Li Mei, Xia Weibo, Xing Xiaopi |
Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome. Blood 2019 7 134 (15): 1227-1237. Brown Austin L, de Smith Adam J, Gant Vincent U, Yang Wenjian, Scheurer Michael E, Walsh Kyle M, Chernus Jonathan M, Kallsen Noah A, Peyton Shanna A, Davies Gareth E, Ehli Erik A, Winick Naomi, Heerema Nyla A, Carroll Andrew J, Borowitz Michael J, Wood Brent L, Carroll William L, Raetz Elizabeth A, Feingold Eleanor, Devidas Meenakshi, Barcellos Lisa F, Hansen Helen M, Morimoto Libby, Kang Alice Y, Smirnov Ivan, Healy Jasmine, Laverdière Caroline, Sinnett Daniel, Taub Jeffrey W, Birch Jillian M, Thompson Pamela, Spector Logan G, Pombo-de-Oliveira Maria S, DeWan Andrew T, Mullighan Charles G, Hunger Stephen P, Pui Ching-Hon, Loh Mignon L, Zwick Michael E, Metayer Catherine, Ma Xiaomei, Mueller Beth A, Sherman Stephanie L, Wiemels Joseph L, Relling Mary V, Yang Jun J, Lupo Philip J, Rabin Karen |
The molecular genetic make-up of male breast cancer. Endocrine-related cancer 2019 Jul . Moelans Cathy B, de Ligt Joep, van der Groep Petra, Prins Pjotr, Besselink Nicolle J M, Hoogstraat Marlous, Ter Hoeve Natalie D, Lacle Miangela M, Kornegoor Robert, van der Pol Carmen C, de Leng Wendy W J, Barbé Ellis, van der Vegt Bert, Martens John, Bult Peter, Smit Vincent T H B M, Koudijs Marco J, Nijman Isaac J, Voest Emile E, Selenica Pier, Weigelt Britta, Reis-Filho Jorge S, van der Wall Elsken, Cuppen Edwin, van Diest Paul |
Clinical and genetic characteristics of hypoparathyroidism in children: a multicenter experience in China. Journal of endocrinological investigation 2024 11 . Yingxiao Shen, Wei Yang, Qin He, Xiaoqin Xu, Yan Sun, Zhihua Wang, Xiaohong Yang, Guanping Dong, Ke Huang, Haiyan Wei, Wei Wu, Junfen |
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