Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Hypophosphatemia and PHEX[original query] |
---|
Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations. Journal of inherited metabolic disease 2018 2 41 (5): 865-876. Chesher Douglas, Oddy Michael, Darbar Ulpee, Sayal Parag, Casey Adrian, Ryan Aidan, Sechi Annalisa, Simister Charlotte, Waters Aoife, Wedatilake Yehani, Lachmann Robin H, Murphy Elai |
Novel variants and uncommon cases among southern Chinese children with X-linked hypophosphatemia. Journal of endocrinological investigation 2020 4 43 (11): 1577-1590. Lin Y, Xu J, Li X, Sheng H, Su L, Wu M, Cheng J, Huang Y, Mao X, Zhou Z, Zhang W, Li C, Cai Y, Wu D, Lu Z, Yin X, Zeng C, Liu |
Prevalence and clinical characteristics of X-linked hypophosphatemia in Paraná, southern Brazil. Archives of endocrinology and metabolism 2020 10 64 (6): 796-802. Moreira Carolina Aguiar, Costa Tatiana M R Lemos, Marques Julia Vieira Oberger, Sylvestre Lucimary, Almeida Ana Cristina R, Maluf Eliane M C P, Borba Victória Z |
A genetic study of a Brazilian cohort of patients with X-linked hypophosphatemia reveals no correlation between genotype and phenotype. Frontiers in pediatrics 2023 10 11 1215952. Mauro Borghi, Leopoldo Muniz da Silva, Luciana Bispo, Carlos A Long |
Disease Manifestations and Complications in Dutch X-Linked Hypophosphatemia Patients. Calcified tissue international 2024 1 . A Bosman, N M Appelman-Dijkstra, A M Boot, M H de Borst, A C van de Ven, R T de Jongh, A Bökenkamp, J P van den Bergh, B C J van der Eerden, M C Zillike |
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 25, 2024
- Content source: