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Gastroenterology|December 1, 1986
Familial visceral neuropathy with autosomal dominant transmissionE A Mayer, M D Schuffler, J I Rotter, et al.Zhonghua Er Bi Yan Hou Ke Za Zhi|May 29, 2003
[Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss]G Xing, X Bu, M Yan, et al.Journal of Chromatography. A|October 16, 2010
Separation of triphenyl atropisomers of a pharmaceutical compound on a novel mixed mode stationary phase: a case study involving dynamic chromatography, dynamic NMR and molecular modelingX Bu, P J Skrdla, P G Dormer, et al.Transplantation Proceedings|June 27, 2006
Significance of C4d deposition in the diagnosis of rejection after liver transplantationX Bu, Z Zheng, Y Yu, et al.Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|January 23, 2020
Regorafenib and ginsenoside combination therapy: inhibition of HepG2 cell growth through modulating survivin and caspase-3 gene expressionB Wang, F Wang, A Ding, et al.American Journal of Otolaryngology|November 1, 1993
Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicityN Fischel-Ghodsian, T R Prezant, X Bu, et al.Gastroenterology|October 1, 1989
Geographic origins of Jewish patients with inflammatory bowel diseaseM P Roth, G M Petersen, C McElree, et al.American Journal of Medical Genetics|July 1, 1994
Increased risk for type I (insulin-dependent) diabetes in relatives of patients with alopecia areata (AA)S J Wang, T Shohat, C Vadheim, et al.Gastroenterology|September 1, 1977
HLA-B5 associated with duodenal ulcerJ I Rotter, D L Rimoin, J M Gursky, et al.American Journal of Human Genetics|November 1, 1982
Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortionB D Blumberg, J D Shulkin, J I Rotter, et al.Pageof 25