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Journal of Medical Genetics|June 25, 2020
Loss of imprinting of the human-specific imprinted gene <i>ZNF597</i> causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndromeKazuki Yamazawa, Takanobu Inoue, Yoshihiro Sakemi, et al.Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|April 22, 2026
Prospective Multicenter Evaluation of the QuickNavi-Campylobacter Assay in Stool SpecimensShinji Hatakeyama, Yumi Hirose, Yusaku Akashi, et al.American Journal of Medical Genetics. Part A|August 18, 2020
Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndromeHiroaki Murakami, Yoshinori Tsurusaki, Keisuke Enomoto, et al.Pageof 6