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BMC Medical Genetics|July 22, 2018
Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairmentIsabelle Schrauwen, Imen Chakchouk, Anushree Acharya, et al.
Clinical and Experimental Dermatology|February 12, 2022
Exome sequencing reveals the first intragenic deletion in ABCA5 underlying autosomal recessive hypertrichosisRubab Raza, Asmat Ullah, Nighat Haider, et al.
Life (Basel, Switzerland)|October 27, 2022
Polyphenols and Their Nanoformulations: Protective Effects against Human DiseasesSantosh Anand, Ramachandregowda Sowbhagya, Mohammad Azam Ansari, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
A locus for hereditary hypotrichosis localized to human chromosome 18q21.1Muhammad Arshad Rafique, Muhammad Ansar, Syed Muhammad Jamal, et al.
Plants (Basel, Switzerland)|March 10, 2022
Quality Control Standardization, Contaminant Detection and In Vitro Antioxidant Activity of <i>Prunus domestica</i> Linn. FruitMohd Amir, Ameeduzzafar Zafar, Rizwan Ahmad, et al.
Human Heredity|December 8, 2004
DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22Muhammad Ansar, Maria H Chahrour, Mohammad Amin Ud Din, et al.
BMC Medical Genetics|December 13, 2007
Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequencesSajid Malik, K M Girisha, Muhammad Wajid, et al.
Current Medicinal Chemistry|July 9, 2021
Epigenetics of Triple-Negative Breast Cancer via Natural CompoundsMohammed Kaleem, Maryam Perwaiz, Suza Mohammad Nur, et al.
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