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Developmental Medicine and Child Neurology|December 19, 2016
Behaviour in Cornelia de Lange syndrome: a systematic reviewPaul A Mulder, Sylvia A Huisman, Raoul C Hennekam, et al.Journal of Child Psychology and Psychiatry, and Allied Disciplines|October 9, 2018
Development, behaviour and autism in individuals with SMC1A variantsPaul A Mulder, Sylvia Huisman, Annemiek M Landlust, et al.Human Genetics|March 21, 2020
Delineation of phenotypes and genotypes related to cohesin structural protein RAD21Lianne C Krab, Iñigo Marcos-Alcalde, Melissa Assaf, et al.American Journal of Medical Genetics. Part A|May 27, 2017
Phenotypes and genotypes in individuals with SMC1A variantsSylvia Huisman, Paul A Mulder, Egbert Redeker, et al.Nature Reviews. Genetics|July 12, 2018
Diagnosis and management of Cornelia de Lange syndrome: first international consensus statementAntonie D Kline, Joanna F Moss, Angelo Selicorni, et al.Human Mutation|June 14, 2018
Further delineation of Malan syndromeManuela Priolo, Denny Schanze, Katrin Tatton-Brown, et al.Pageof 1