Showing results (1-10 of 3) with videos related to
Sort By:
Pageof 1
Genetic Counseling (Geneva, Switzerland)|August 19, 2011
A novel mutation of the claudin 16 gene in familial hypomagnesemia with hypercalciuria and nephrocalcinosis mimicking ricketsC S Kasapkara, L Tumer, I Okur, et al.Genetic Counseling (Geneva, Switzerland)|April 25, 2013
An extremely rare case: osteosclerotic metaphyseal dysplasiaC S Kasapkara, A Küçükçongar, O Boyunağa, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 14, 2012
SRD5A3-CDG: a patient with a novel mutationC S Kasapkara, L Tümer, F S Ezgü, et al.Pageof 1