Associated Papers
Clinical and Genetic Characteristics of Patients with Unexplained Intellectual Disability/Developmental Delay without Epilepsy.
Gerik-Celebi HB et al.
Molecular Syndromology, 2023
Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome.
Li M et al.
European Journal of Human Genetics : Ejhg, 2016
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