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Laboratory Animals|February 8, 2002
Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless geneWasim Ahmad, Marion S Ratterree, Andrei A Panteleyev, et al.
Immunobiology|April 14, 2020
β2 Integrin Gene (ITGB2) mutation spectra in Pakistani families with leukocyte adhesion deficiency type 1 (LAD1)Hamid Nawaz Tipu, Rubab Raza, Sadaf Jaffar, et al.
European Journal of Medical Genetics|October 6, 2022
A novel homozygous variant in homologous recombination repair gene ZSWIM7 causes azoospermia in males and primary ovarian insufficiency in femalesShah Hussain, Shoaib Nawaz, Ihsan Khan, et al.
Pakistan Journal of Pharmaceutical Sciences|November 28, 2017
Report: Potential of nano-emulsions as phytochemical delivery system for food preservationZaffar Mahmood, Muhammad Jahangir, Muhammad Liaquat, et al.
Congenital Anomalies|September 1, 2016
Novel homozygous sequence variants in the GDF5 gene underlie acromesomelic dysplasia type-grebe in consanguineous familiesMuhammad Umair, Afzal Rafique, Asmat Ullah, et al.
Discover Oncology|September 29, 2025
Exploring drug repurposing for PAK2 inhibition: a systematic virtual screening of FDA-approved drugs against cancerShadma Wahab, Abdulrhman Alsayari, Taghreed A Majrashi, et al.
Jornal De Pediatria|September 4, 2017
Cerebrospinal fluid lactate: a differential biomarker for bacterial and viral meningitis in childrenMudasir Nazir, Wasim Ahmad Wani, Muzaffar Ahmad Malik, et al.
Molecular Syndromology|June 16, 2023
Sequence Variants in <i>MEGF8</i> and <i>GJA1</i> Underlying SyndactylyMuhammad Bilal, Tobias B Haack, Rebecca Buchert, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 21, 2008
Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patientsMuhammad J Hassan, Saqib Mahmood, Ghazanfar Ali, et al.
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