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Journal of Human Genetics|February 9, 2010
Prediction of the clinical phenotype of Fabry disease based on protein sequential and structural informationSeiji Saito, Kazuki Ohno, Jun Sese, et al.
Journal of Human Genetics|July 29, 2018
Genome-wide association study suggests four variants influencing outcomes with ranibizumab therapy in exudative age-related macular degenerationMasato Akiyama, Atsushi Takahashi, Yukihide Momozawa, et al.
Journal of Human Genetics|July 19, 2018
A novel SLC9A1 mutation causes cerebellar ataxiaKazuhiro Iwama, Hitoshi Osaka, Takahiro Ikeda, et al.
Journal of Human Genetics|August 17, 2018
Contribution of RAD51D germline mutations in breast and ovarian cancer in GreeceIrene Konstanta, Florentia Fostira, Paraskevi Apostolou, et al.
Journal of Human Genetics|March 13, 2010
Factor V Leiden mutation in Arabs in Kuwait by real-time PCR: different values for different ArabsAli A Dashti, Mehrez M Jadaon, Hend L Lewis
Journal of Human Genetics|June 9, 2017
Maternally derived 15q11.2-q13.1 duplication and H19-DMR hypomethylation in a patient with Silver-Russell syndromeSumito Dateki, Masayo Kagami, Keiko Matsubara, et al.
Journal of Human Genetics|April 26, 2018
An estimation of the prevalence of genomic disorders using chromosomal microarray dataMadelyn A Gillentine, Philip J Lupo, Pawel Stankiewicz, et al.
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