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Human Genetics|October 1, 1986
Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1C Turleau, F Taillard, M Doussau de Bazignan, et al.Human Genetics|December 1, 1986
A linkage study of Emery-Dreifuss muscular dystrophyS Hodgson, E Boswinkel, C Cole, et al.Human Genetics|January 28, 2022
Heat increases full-length SMN splicing: promise for splice-augmenting therapies for SMACatherine E Dominguez, David Cunningham, Akila S Venkataramany, et al.Human Genetics|January 31, 2022
Evaluating the relevance of sequence conservation in the prediction of pathogenic missense variantsEmidio Capriotti, Piero FariselliHuman Genetics|November 1, 1986
Chromosome changes in human monocytic cell lines with in vitro spontaneous malignant transformationL Romitti, R P Revoltella, E Vigneti, et al.Human Genetics|November 1, 1986
Effect of the esterase-D phenotype on its in vitro enzyme activityJ K Cowell, P Rutland, M Jay, et al.Human Genetics|October 2, 2021
Clinical implementation of drug metabolizing gene-based therapeutic interventions worldwideEvangelia Eirini Tsermpini, Zeina N Al-Mahayri, Bassam R Ali, et al.Human Genetics|February 19, 2022
Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylationEline Blommaert, Natalia A Cherepanova, Frederik Staels, et al.Human Genetics|January 24, 2022
Analysis of histone variant constraint and tissue expression suggests five potential novel human disease genes: H2AFY2, H2AFZ, H2AFY, H2AFV, H1F0Emily Lubin, Laura Bryant, Joseph Aicher, et al.Human Genetics|April 1, 1987
Mammalian T-lymphocyte antigen receptor genes: genetic and nongenetic potential to generate variabilityJ T Epplen, J Chluba, C Hardt, et al.Pageof 959