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Molecular Genetics & Genomic Medicine|March 22, 2021
Panel-based genetic testing for inherited retinal disease screening 176 genesLeo H N Sheck, Simona D Esposti, Omar A Mahroo, et al.
Molecular Genetics & Genomic Medicine|December 29, 2021
A Leigh syndrome caused by compound heterozygous mutations on NDUFAF5 induce early infant death: A case reportYan Wen, Guoyan Lu, Lina Qiao, et al.
Molecular Genetics & Genomic Medicine|February 7, 2022
New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3, CSMD1 and NRG1 genesSouhir Mestiri, Sami Boussetta, Andrew J Pakstis, et al.
Molecular Genetics & Genomic Medicine|February 12, 2022
Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variantThashi Bharadwaj, Isabelle Schrauwen, Anushree Acharya, et al.
Molecular Genetics & Genomic Medicine|June 21, 2019
STAT3 signaling pathway plays importantly genetic and functional roles in HCV infectionYuzhu Song, Xianyao Yang, Yunsong Shen, et al.
Molecular Genetics & Genomic Medicine|July 4, 2019
Haplotype analysis of SERPINE1 gene: Risk for aneurysmal subarachnoid hemorrhage and clinical outcomesMingkuan Lin, Christoph J Griessenauer, Robert M Starke, et al.
Molecular Genetics & Genomic Medicine|February 22, 2022
Genetic analysis and clinical significance of a rare t(1;12)(q21;p13) in a patient with high-risk myelodysplastic syndromeFang Fang, Ru Jia, Congyan Liu, et al.
Molecular Genetics & Genomic Medicine|February 11, 2022
Autosomal recessive monilethrix: Novel variants of the DSG4 gene in three Chinese familiesCheng Zhou, Pei Wang, Dingquan Yang, et al.
Molecular Genetics & Genomic Medicine|February 12, 2022
Mdr3 gene mutation in preterm infants with parenteral nutrition-associated cholestasisXiufang Yang, Guosheng Liu, Bing Yi
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