Found 2 results
Filters: Keyword is Humans and Author is Fryns, J P [Clear All Filters]
"Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene.", Hum Mol Genet, vol. 9, issue 9, pp. 1321-8, 2000 May 22.
"A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy.", Clin Genet, vol. 52, issue 3, pp. 135-41, 1997 Sep.