Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.

B B de Vries; J P Fryns; M G Butler; F Canziani; E Wesby-van Swaay; J O van Hemel; B A Oostra; D J Halley; M F Niermeijer

doi:10.1136/jmg.30.9.761

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Research Article

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.

Authors

B B de Vries PubMed articles Google scholar articles
J P Fryns PubMed articles Google scholar articles
M G Butler PubMed articles Google scholar articles
F Canziani PubMed articles Google scholar articles
E Wesby-van Swaay PubMed articles Google scholar articles
J O van Hemel PubMed articles Google scholar articles
B A Oostra PubMed articles Google scholar articles
D J Halley PubMed articles Google scholar articles
M F Niermeijer PubMed articles Google scholar articles

Citation

de Vries BB, Fryns JP, Butler MG, et al

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.

Journal of Medical Genetics 1993;30:761-766.

Publication history

First published September 1, 1993.

Online issue publication

April 27, 2016

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