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American Journal of Medical Genetics|May 30, 1998
Craniometadiaphyseal dysplasia, wormian bone typeJ M Santolaya, C M Hall, S García-Miñaur, et al.
Placenta|April 24, 2009
CDKN1C mutations in HELLP/preeclamptic mothers of Beckwith-Wiedemann Syndrome (BWS) patientsV Romanelli, A Belinchón, A Campos-Barros, et al.
Cirugia Pediatrica : Organo Oficial De La Sociedad Espanola De Cirugia Pediatrica|April 13, 1999
[Integrated treatment of cleft lip and palate. Organization of a treatment team]I Sánchez-Ruiz, G González Landa, V Pérez González, et al.
Human Mutation|March 17, 2010
FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletionsB D'haene, J Nevado, M Pugeat, et al.
Clinical Genetics|September 12, 2017
mTOR mutations in Smith-Kingsmore syndrome: Four additional patients and a reviewG Gordo, J Tenorio, P Arias, et al.
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