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Clinical Genetics|November 11, 2010
Paternal mosaicism of an STXBP1 mutation in OSH Saitsu, H Hoshino, M Kato, et al.Clinical Genetics|May 26, 2018
PRUNE1-related disorder: Expanding the clinical spectrumE Imagawa, Y Yamamoto, S Mitsuhashi, et al.Nihon Jinzo Gakkai Shi|August 1, 1996
[Clinical investigation of 10 cases with acute renal failure induced by neuroleptics]A Soejima, M Suzuki, S Ishizuka, et al.Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|May 1, 2009
Role of endoscopic ultrasonography in predicting the response to cyclosporin A in ulcerative colitis refractory to steroidsO Watanabe, T Ando, E M El-Omar, et al.Clinical Genetics|February 27, 2016
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?A Fujita, C Waga, Y Hachiya, et al.Cell Death and Differentiation|April 28, 2007
Novel role of HDAC inhibitors in AML1/ETO AML cells: activation of apoptosis and phagocytosis through induction of annexin A1Y Tabe, L Jin, R Contractor, et al.International Journal of Immunogenetics|March 9, 2011
Exonic deletion of CASP10 in a patient presenting with systemic juvenile idiopathic arthritis, but not with autoimmune lymphoproliferative syndrome type IIaH Tadaki, H Saitsu, H Kanegane, et al.Clinical Genetics|March 27, 2015
Delineation of clinical features in Wiedemann-Steiner syndrome caused by KMT2A mutationsN Miyake, Y Tsurusaki, E Koshimizu, et al.Clinical Genetics|May 31, 2017
Novel biallelic SZT2 mutations in 3 cases of early-onset epileptic encephalopathyN Tsuchida, M Nakashima, A Miyauchi, et al.Pageof 9