Associated Papers
Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.
Dworschak GC et al.
Orphanet Journal of Rare Diseases, 2021
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.
Al-Mubarak B et al.
Scientific Reports, 2017
28720891 (PubMed )
Supplement: 41598_2017_6033_MOESM1_ESM.pdf
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