Molecular Analysis of the Retinoic Acid Induced 1 Gene (RAI1) in Patients with Suspected Smith-Magenis Syndrome without the 17p11.2 Deletion
Thierry Vilboux(Inova Health System), Marjan Huizing(National Human Genome Research Institute), Wendy J. Introne, Ann C. M. Smith(Children's Hospital Colorado), Jan Blancato(Georgetown University), William A. Gahl(National Institute of Child Health), Gerald F. Cox(Harvard University Press), Carla Ciccone(National Institutes of Health), Charu Deshpande(Guy's Hospital)
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