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Plos One|December 19, 2023
An application of fuzzy bipolar weighted correlation coefficient in decision-making problemSaima Mustafa, Sadia Mahmood, Zabidin SallehEntropy (Basel, Switzerland)|December 3, 2020
Analytical Solutions of Fractional-Order Diffusion Equations by Natural Transform Decomposition MethodRasool Shah, Hassan Khan, Saima Mustafa, et al.Genes & Genomics|June 8, 2020
A novel nonsense mutation in NPR2 gene causing Acromesomelic dysplasia, type Maroteaux in a consanguineous family in Southern Punjab (Pakistan)Saima Mustafa, Zafrin Akhtar, Muhammad Latif, et al.International Ophthalmology|June 1, 2017
Association of Single Nucleotide Polymorphisms in XRCC1 (194) and XPD (751) with Age-related cataractTafheem Khosa, Sana Aslam, Saima Mustafa, et al.JPMA. the Journal of the Pakistan Medical Association|January 27, 2018
Association of single nucleotide polymorphism in CD28(C/T-I3 + 17) and CD40 (C/T-1) genes with the Graves' diseaseSaima Mustafa, Hira Fatima, Sadia Fatima, et al.Genes|November 24, 2022
A Missense Mutation (c.1037 G > C, p. R346P) in <i>PAPSS2</i> Gene Results in Autosomal Recessive form of Brachyolmia Type 1 (Hobaek Form) in A Consanguineous FamilySaima Mustafa, Malik Fiaz Hussain, Muhammad Latif, et al.European Journal of Medical Genetics|May 30, 2020
A novel homozygous missense variant in MATN3 causes spondylo-epimetaphyseal dysplasia Matrilin 3 type in a consanguineous familySamina Yasin, Saima Mustafa, Arzoo Ayesha, et al.Heredity|December 14, 2017
A missense point mutation in COL10A1 identified with whole-genome deep sequencing in a 7-generation Pakistan dwarf familyChao Zhang, Jiaojiao Liu, Furhan Iqbal, et al.Pageof 1