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- The association of chromosome 3 duplication and the Correlia de...
Golder N., Wilson , Virginia C., Hieber , Roy D., Schmickel... - Deletion of 8p23.1 with features of Cornelia de Lange syndrome and...
12, p. 1565-70, 35 refs, ISSN: 1552-4833. Abstract. Cornelia de Lange syndrome (CdLS) is characterized by facial dysmorphism; hirsutism; - Cochlear implantation in children with Jervell, Lange-Nielsen...
Related Articles Cochlear implantation in children with Jervell, Lange-Nielsen syndrome. J Laryngol Otol. 2008 Mar;122(3):314-7... - Incidence and clinical features of X-linked Cornelia de Lange...
Cornelia de Lange syndrome (CdLS) is a multisystem developmental disorder characterized by facial dysmorphism, growth and mental retardation, - Mutations in cohesin complex members SMC3 and SMC1A cause a mild...
...cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively. - CdLS, Cornelia de Lange Syndrome, Canada
Read and post comments | Send to a friend... - The behavioural phenotype of Cornelia de Lange Syndrome: a study of...
Journal of Intellectual Disability Research; 09/01/2007... - Infant attentional behaviours as prognostic indicators in...
Journal of Intellectual Disability Research; 09/01/2007... - May 10th is Cornelia de Lange Syndrome Awareness...
This Saturday we will celebrate CdLS Awareness Day! ... life. - Prevalence of autism spectrum phenomenology in cornelia de lange and...
...administered to 34 participants with Cornelia de Lange syndrome and a comparison group of 23 participants with Cri du Chat syndrome (M ages 12...