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Molecular Genetics & Genomic Medicine|November 28, 2017
Mutations in fetal genes involved in innate immunity and host defense against microbes increase risk of preterm premature rupture of membranes (PPROM)Bhavi P Modi, Maria E Teves, Laurel N Pearson, et al.Molecular Genetics & Genomic Medicine|November 28, 2017
RYR1 causing distal myopathyRuple S Laughlin, Zhiyv Niu, Eric Wieben, et al.Molecular Genetics & Genomic Medicine|December 24, 2017
A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathyIlona Schirmer, Mareike Dieding, Bärbel Klauke, et al.Molecular Genetics & Genomic Medicine|December 2, 2017
Association of MGMT promoter methylation with tumorigenesis features in patients with ovarian cancer: A systematic meta-analysisBaoli Qiao, Zhenyu Zhang, Yanfang LiMolecular Genetics & Genomic Medicine|March 8, 2018
Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish familiesKawther Taleb, Eva Lauridsen, Jette Daugaard-Jensen, et al.Molecular Genetics & Genomic Medicine|February 15, 2018
Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3ARicardo A Maselli, Jessica Vázquez, Leah Schrumpf, et al.Molecular Genetics & Genomic Medicine|May 7, 2018
Alpha-synuclein mRNA isoform formation and translation affected by polymorphism in the human SNCA 3'UTRElizabeth S Barrie, Sung-Ha Lee, John T Frater, et al.Molecular Genetics & Genomic Medicine|May 9, 2018
Next generation sequencing panel based on single molecule molecular inversion probes for detecting genetic variants in children with hypopituitarismMaría I Pérez Millán, Sebastian A Vishnopolska, Alexandre Z Daly, et al.Molecular Genetics & Genomic Medicine|May 27, 2017
Uniparental disomy determined by whole-exome sequencing in a spectrum of rare motoneuron diseases and ataxiasDana M Bis, Rebecca Schüle, Jennifer Reichbauer, et al.Molecular Genetics & Genomic Medicine|May 27, 2017
A birth of bipartite exon by intragenic deletionKandai Nozu, Kazumoto Iijima, Toru Igarashi, et al.Pageof 252