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Gene|September 12, 2012
Detection of common mutations in the GALT gene through ARMSUmair Mahmood, Muhammad Imran, Salma Iqbal Naik, et al.
Case Reports in Perinatal Medicine|May 5, 2025
Aromatase deficiency due to novel CYP19A1 mutation: a rare cause of maternal and fetal virilizationAamir Naseem, Muhammad Zahid, Kashan Arshad, et al.
Hormone Research in Paediatrics|August 25, 2025
Clinical Spectrum of Primary Hypomagnesemia with Secondary Hypocalcemia due to TRPM6 MutationSommayya Aftab, Muhammad Nadeem Anjum, Nida Aslam, et al.
The Turkish Journal of Gastroenterology : the Official Journal of Turkish Society of Gastroenterology|August 21, 2023
Clinical and Genetic Description of Hereditary Chronic Pancreatitis in Pakistani ChildrenHuma Arshad Cheema, Zafar Fayyaz, Anjum Saeed, et al.
JPMA. the Journal of the Pakistan Medical Association|January 2, 2022
Very early onset inflammatory bowel disease: Spectrum of clinical presentation, diagnostic tools and outcome in childrenHuma Arshad Cheema, Nadia Waheed, Anjum Saeed, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|July 17, 2017
Spontaneous Perforation Of Bile Duct, Clinical Presentation, Laboratory Work Up, Treatment And OutcomeHassan Suleman Malik, Huma Arshad Cheema, Zafar Fayyaz, et al.
Bioengineering (Basel, Switzerland)|December 23, 2022
Phyto-Synthesis, Characterization, and In Vitro Antibacterial Activity of Silver Nanoparticles Using Various Plant ExtractsBilal Ahmad, Li Chang, Usama Qamar Satti, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 21, 2024
Diabetes and CFAP126 gene mutation; are they really linked together?Kashan Arshad, Aamir Naseem, Syed Saddam Hussain, et al.
Plant Physiology and Biochemistry : PPB|May 13, 2024
The role of reduced graphene oxide on mitigation of lead phytotoxicity in Triticum aestivum L.plants at morphological and physiological levelsQingying Zhan, Ashfaq Ahmad, Huma Arshad, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 14, 2015
Direct sequencing of FAH gene in Pakistani tyrosinemia type 1 families reveals a novel mutationSadaqat Ijaz, Muhammad Yasir Zahoor, Muhammad Imran, et al.
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