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Plos One|February 6, 2013
Germline allele-specific expression of DAPK1 in chronic lymphocytic leukemiaQuan-Xiang Wei, Rainer Claus, Thomas Hielscher, et al.Clinical Kidney Journal|April 13, 2018
Intensive haemodialysis using PMMA dialyser does not increase renal response rate in multiple myeloma patients with acute kidney injuryLaurent Hudier, Olivier Decaux, Atmann Haddj-Elmrabet, et al.Journal of Medical Genetics|January 8, 2008
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndromeM Clendenning, L Senter, H Hampel, et al.Genome Research|March 1, 1996
Construction of a 750-kb bacterial clone contig and restriction map in the region of human chromosome 21 containing the progressive myoclonus epilepsy geneN E Stone, J B Fan, V Willour, et al.Cancer|January 1, 1996
Genetic counseling in a Navajo hereditary nonpolyposis colorectal cancer kindredH T Lynch, T Drouhard, H F Vasen, et al.European Journal of Human Genetics : EJHG|July 12, 2002
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retinaKrisztina Wutz, Christian Sauer, Eberhart Zrenner, et al.Protein Science : a Publication of the Protein Society|March 8, 2016
Structural characterization of NRAS isoform 5Joseph Markowitz, Tapas K Mal, Chunhua Yuan, et al.Journal of Sleep Research|February 1, 2025
Dreaming in patients with epilepsy: a cross-sectional cohort studyMaïlis Charpentier-Hélary, Aurélien de la Chapelle, Maxime Linard, et al.Cell|February 24, 2001
Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasiaM Ridanpää, H van Eenennaam, K Pelin, et al.Human Molecular Genetics|November 5, 1997
Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated populationT Laitinen, P Kauppi, J Ignatius, et al.Pageof 61