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American Journal of Medical Genetics. Part A|January 8, 2005
Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31Asif Mir, Muhammad Ansar, Maria H Chahrour, et al.
The Journal of Gene Medicine|September 27, 2023
Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmiaWarda Akbar, Asmat Ullah, Nighat Haider, et al.
Frontiers in Genetics|August 12, 2024
Management of triple-negative breast cancer by natural compounds through different mechanistic pathwaysMohammed Kaleem, Mandar Thool, Nitin G Dumore, et al.
Saudi Medical Journal|December 7, 2017
Novel duplication mutation of the DYSF gene in a Pakistani family with Miyoshi MyopathyMuhammad I Ullah, Arsalan Ahmad, Milena Zarkovic, et al.
Plants (Basel, Switzerland)|January 11, 2022
Pharmacological Efficacy of <i>Tamarix aphylla</i>: A Comprehensive ReviewSaad Ali Alshehri, Shadma Wahab, Shahabe Saquib Abullais, et al.
American Journal of Medical Genetics. Part A|March 25, 2004
A novel type of autosomal recessive syndactyly: clinical and molecular studies in a family of Pakistani originSajid Malik, Muhammad Arshad, Muhammad Amin-Ud-Din, et al.
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