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Congenital Anomalies|October 18, 2019
Novel heterozygous sequence variant in the GLI1 underlies postaxial polydactylyMaryam Yousaf, Asmat Ullah, Zahid Azeem, et al.BMC Medical Genomics|December 19, 2024
THBS1 is a new autosomal recessive non-syndromic hearing impairment geneThashi Bharadwaj, Anushree Acharya, Fati Ullah Khan, et al.Journal of Maxillofacial and Oral Surgery|October 8, 2024
Role of Whey Protein in the Treatment Outcome of Maxillofacial Trauma Patients: An Interventional StudyWasim Ahmad, Sajjad Abdur Rahman, Ghulam Sarwar Hashmi, et al.Genetics Research International|May 9, 2012
Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX GeneKwanghyuk Lee, Mohammad Amin Ud Din, Muhammad Ansar, et al.Molecular Immunology|December 8, 2014
Association analysis of GWAS and candidate gene loci in a Pakistani population with psoriasisSaeeda Munir, Simeen ber Rahman, Sadia Rehman, et al.Archives of Dermatological Research|June 14, 2006
Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi originsPeter John, Muhammad Tariq, Muhammad Arshad Rafiq, et al.American Journal of Medical Genetics. Part A|January 17, 2012
Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing lossKwanghyuk Lee, Muhammad Ansar, Paula B Andrade, et al.Journal of Molecular Medicine (Berlin, Germany)|April 6, 2006
Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2-q13.32Aamira Tariq, Regie Lyn P Santos, Mohammad Nasim Khan, et al.Journal of Biomolecular Structure & Dynamics|December 20, 2023
Phytochemicals as potential inhibitors of interleukin-8 for anticancer therapy: <i>in silico</i> evaluation and molecular dynamics analysisMohammad Y Alshahrani, Ali Gaithan Alkhathami, Mohammad Ali Abdullah Almoyad, et al.Frontiers in Pediatrics|January 31, 2020
A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani FamilyAmjad Khan, Rongrong Wang, Shirui Han, et al.Pageof 34