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American Journal of Medical Genetics. Part A|May 21, 2013
Familial trisomy 6p in mother and daughterMarco Savarese, Anna Grandone, Lucia Perone, et al.American Journal of Medical Genetics. Part A|August 2, 2005
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization of 11 casesManuela Morleo, Tiziano Pramparo, Lucia Perone, et al.Human Molecular Genetics|September 17, 2011
The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome casesNicoletta Chiesa, Agostina De Crescenzo, Kankadeb Mishra, et al.Hormone Research in Paediatrics|October 27, 2016
Multiplex Ligation-Dependent Probe Amplification Accurately Detects Turner Syndrome in Girls with Short StatureAnna Grandone, Francesca Del Vecchio Blanco, Annalaura Torella, et al.Pageof 2