Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.
de Vries, B B, Fryns, J P, Butler, M G, Canziani, F, Wesby-van Swaay, E, van Hemel, J O, Oostra, B A, Halley, D J, Niermeijer, M FVolume:
30
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.30.9.761
Date:
September, 1993
File:
PDF, 2.00 MB
english, 1993