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Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families.
Doll J, Vona B, Schnapp L, Rüschendorf F, Khan I, Khan S, Muhammad N, Alam Khan S, Nawaz H, Khan A, Ahmad N, Kolb SM, Kühlewein L, Labonne JDJ, Layman LC, Hofrichter MAH, Röder T, Dittrich M, Müller T, Graves TD, Kong IK, Nanda I, Kim HG, Haaf T. Doll J, et al. Among authors: alam khan s. Genes (Basel). 2020 Nov 11;11(11):1329. doi: 10.3390/genes11111329. Genes (Basel). 2020. PMID: 33187236 Free PMC article.
Detection of Novel Biallelic Causative Variants in COL7A1 Gene by Whole-Exome Sequencing, Resulting in Congenital Recessive Dystrophic Epidermolysis Bullosa in Three Unrelated Families.
Fozia F, Nazli R, Alrashed MM, Ghneim HK, Haq ZU, Jabeen M, Alam Khan S, Ahmad I, Bourhia M, Aboul-Soud MAM. Fozia F, et al. Among authors: alam khan s. Diagnostics (Basel). 2022 Jun 23;12(7):1525. doi: 10.3390/diagnostics12071525. Diagnostics (Basel). 2022. PMID: 35885431 Free PMC article.