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

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

Identifier:nobleid.org/w1/20260515/069DA30C

Type:Journal Article

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

Identifier:nobleid.org/w1/20260515/069DA30C

Type:Journal Article

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