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Surgery Today|July 7, 2000
Identification of high-risk breast cancer patients from genetic changes of their tumorsM Watatani, H Inui, K Nagayama, et al.Nature Genetics|June 1, 1992
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1AN Matsunami, B Smith, L Ballard, et al.Cancer Chemotherapy and Pharmacology|May 30, 2014
A phase II study of metronomic paclitaxel/cyclophosphamide/capecitabine followed by 5-fluorouracil/epirubicin/cyclophosphamide as preoperative chemotherapy for triple-negative or low hormone receptor expressing/HER2-negative primary breast cancerN Masuda, K Higaki, T Takano, et al.Genomics|December 1, 1993
A somatic cell hybrid map of human chromosome 13S S Washington, A M Bowcock, S Gerken, et al.Molecular Psychiatry|February 20, 2008
A high-density SNP genome-wide linkage scan in a large autism extended pedigreeK Allen-Brady, J Miller, N Matsunami, et al.Cell|January 15, 1993
DNA deletion associated with hereditary neuropathy with liability to pressure palsiesP F Chance, M K Alderson, K A Leppig, et al.Genes and Immunity|July 25, 2008
Detailed genetic characterization of the interleukin-23 receptor in psoriasisV E Garcia, M Chang, R Brandon, et al.Genes and Immunity|December 14, 2007
Variants in the 5q31 cytokine gene cluster are associated with psoriasisM Chang, Y Li, C Yan, et al.Neuroimage. Clinical|February 1, 2017
Multivariate characterization of white matter heterogeneity in autism spectrum disorderD C Dean, N Lange, B G Travers, et al.Pageof 4