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Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome.
Genes (Basel). 2023 May 19;14(5):1113. doi: 10.3390/genes14051113.
Genes (Basel). 2023.
PMID: 37239474
Free PMC article.
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: nawaz h.
Genes (Basel). 2020 Nov 11;11(11):1329. doi: 10.3390/genes11111329.
Genes (Basel). 2020.
PMID: 33187236
Free PMC article.
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Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients.
Nawaz H, Parveen A, Khan SA, Zalan AK, Khan MA, Muhammad N, Hassib NF, Mostafa MI, Elhossini RM, Roshdy NN, Ullah A, Arif A, Khan S, Ammerpohl O, Wasif N.
Nawaz H, et al.
Heliyon. 2023 Dec 14;10(1):e23688. doi: 10.1016/j.heliyon.2023.e23688. eCollection 2024 Jan 15.
Heliyon. 2023.
PMID: 38192829
Free PMC article.
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