Human Genome Epidemiology Literature Finder
|
Records 1 - 3 (of 3 Records) |
| Query Trace: Syndrome and THRB[original query] |
|---|
| Clinical and Molecular Characteristics of Eight Israeli Families with Thyroid Hormone Receptor Beta Mutations. The Israel Medical Association journal : IMAJ 2018 11 20 (11): 679-686. Zaig Eliyahu, Cohen-Ouaknine Odile, Tsur Anat, Nagar Sheila, Bril Gherta, Tolkin Lior, Cahn Avivit, Heyman Mozhgan, Glaser Benjam |
| Apparent resistance to thyroid hormones: From biological interference to genetics. Annales d'endocrinologie 2019 10 80 (5-6): 280-285. Dieu Xavier, Sueur Guillaume, Moal Valérie, Boux de Casson Florence, Bouzamondo Nathalie, Bouhours Natacha, Briet Claire, Illouz Frédéric, Reynier Pascal, Coutant Régis, Rodien Patrice, Mirebeau-Prunier Delphi |
| THRB Gene Mosaicism Confirmed by Next-Generation Sequencing in a Clinically Symptomatic Infant. JCEM case reports 2024 5 2 (5): luae075. Jenny Yeuk Ki Cheng, Shreenidhi Ranganatha Subramaniam, Hoi Shan Leung, Sammy Wai Chun Wong, Jeffrey Sung Shing Kwok, Wai Kei Jacky L |
- Page last reviewed:Feb 1, 2024
- Content source:

