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Journal of Medical Genetics|December 15, 2016
Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of <i>KRT83</i> and is allelic with dominant monilethrixKhadim Shah, Muhammad Ansar, Zaib-Un-Nisa Mughal, et al.
Genetic Testing and Molecular Biomarkers|October 2, 2019
Variants in <i>GLI3</i> Cause Greig Cephalopolysyndactyly SyndromeAbdullah, Maryam Yousaf, Zahid Azeem, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12Muhammad Wajid, Amir Ali Abbasi, Muhammad Ansar, et al.
Journal of Medical Genetics|November 20, 2012
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type AUmm-e- Kalsoom, Eva Klopocki, Naveed Wasif, et al.
Human Heredity|August 2, 2003
Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from PakistanMuhammad Ansar, Mohammad Ramzan, Thanh L Pham, et al.
Molecules (Basel, Switzerland)|December 24, 2015
Storage Stability of Kinnow Fruit (Citrus reticulata) as Affected by CMC and Guar Gum-Based Silver Nanoparticle CoatingsSyed Wasim Ahmad Shah, Muhammad Jahangir, Muhammad Qaisar, et al.
Medicina (Kaunas, Lithuania)|February 25, 2023
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in <i>CYB5R3</i> Gene in Patients with MethemoglobinemiaAsmat Ullah, Abid Ali Shah, Fibhaa Syed, et al.
Plants (Basel, Switzerland)|September 28, 2021
Morusflavone, a New Therapeutic Candidate for Prostate Cancer by CYP17A1 Inhibition: Exhibited by Molecular Docking and Dynamics SimulationSayed Aliul Hasan Abdi, Amena Ali, Shabihul Fatma Sayed, et al.
International Journal of Dermatology|December 19, 2015
Disease causing homozygous variants in the human hairless geneSabba Mehmood, Abid Jan, Syed Irfan Raza, et al.
Genes|June 27, 2020
Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing ImpairmentIsabelle Schrauwen, Khurram Liaqat, Isabelle Schatteman, et al.
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