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17. High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families. AlAyadhi LY; Hashmi JA; Iqbal M; Albalawi AM; Samman MI; Elamin NE; Bashir S; Basit S Neuroscience; 2016 Dec; 339():561-570. PubMed ID: 27771533 [TBL] [Abstract][Full Text] [Related]
18. A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents. Knijnenburg J; Oberstein SA; Frei K; Lucas T; Gijsbers AC; Ruivenkamp CA; Tanke HJ; Szuhai K J Med Genet; 2009 Jun; 46(6):412-7. PubMed ID: 19246478 [TBL] [Abstract][Full Text] [Related]