Showing results (1-10 of 935) with videos related to
Sort By:
Pageof 94
Genes|September 23, 2022
A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani FamilyHammad Yousaf, Ambrin Fatima, Zafar Ali, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 16, 2011
The Wilson films--MS tremorMathias ToftFrontiers in Pediatrics|June 1, 2026
A homozygous splice-site variant in SAMHD1 shows variable expressivity of Aicardi-Goutières syndrome type 5: a case report and literature reviewHammad Yousaf, Zehra Zonash, Javeria Manzoor, et al.Asian Pacific Journal of Cancer Prevention : APJCP|May 30, 2014
Molecular genetic studies on 167 pediatric ALL patients from different areas of Pakistan confirm a low frequency of the favorable prognosis fusion oncogene TEL-AML1 (t 12; 21) in underdeveloped countries of the regionZafar IqbalIndian Journal of Human Genetics|June 25, 2014
A comprehensive analysis of breakpoint cluster region-abelson fusion oncogene splice variants in chronic myeloid leukemia and their correlation with disease biologyZafar IqbalCellular and Molecular Biology (Noisy-Le-Grand, France)|April 26, 2025
Spatial distribution and genetic diversity of TYLCV in Saudi ArabiaZafar IqbalViruses|December 31, 2025
Contrasting Evolutionary Dynamics and Global Dissemination of the DNA-A and DNA-B Components of Watermelon Chlorotic Stunt VirusZafar IqbalNeurogenetics|July 30, 2011
Genetic variability in SNCA and Parkinson's diseaseLasse Pihlstrøm, Mathias ToftPlos One|October 13, 2017
Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegiaZafar Iqbal, Siri L Rydning, Iselin M Wedding, et al.Pageof 94