Results 231 to 236 of about 6,876 (236)

Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic rickets

Journal of Human Genetics, 2012
Kim Brixen, Jeppe Gram, Klaus Brusgaard
exaly  

Growth in PHEX-associated X-linked hypophosphatemic rickets: the importance of early treatment

Pediatric Nephrology, 2011
Catherine Quinlan, Amaka C Offiah, Sian Ellard   +2 more
exaly  

Novel and de novo PHEX mutations in patients with hypophosphatemic rickets

Bone, 2013
Brian F Meyer, Yufei Shi
exaly  

Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic rickets

Bone, 2019
Brian F Meyer, Yufei Shi
exaly  

Die Rolle des PHEX-Gens in der Phosphathomöostase

2004
openaire   +1 more source

Mutational analysis of PHEX, FGF23 and DMP1 in a cohort of patients with hypophosphatemic rickets

Clinical Endocrinology, 2011
exaly