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Medical Reference Services Quarterly|January 24, 2017
Managing and Coding References for Systematic Reviews and Scoping Reviews in EndNoteMicah D J PetersKidney International|November 1, 1990
Congenital hepatic fibrosis in autosomal-dominant polycystic kidney diseaseJ M Cobben, M H Breuning, C Schoots, et al.Leukemia|February 1, 1996
Acute myelogenous leukemia: a disorder of gene splicing?B A van der Reijden, G J van Ommen, A Hagemeijer, et al.Human Genetics|July 1, 1993
Icelandic families with autosomal dominant polycystic kidney disease: families unlinked to chromosome 16p13.3 revealed by linkage analysisR Fossdal, M Böthvarsson, P Asmundsson, et al.Human Molecular Genetics|November 1, 1992
Multiple colors by fluorescence in situ hybridization using ratio-labelled DNA probes create a molecular karyotypeJ G Dauwerse, J Wiegant, A K Raap, et al.Nederlands Tijdschrift Voor Geneeskunde|February 26, 2005
[From gene to disease; from CLN1, CLN2 and CLN3 to neuronal ceroid lipofuscinosis]P E M Taschner, M Losekoot, M H Breuning, et al.Science (New York, N.Y.)|May 31, 1996
PKD2, a gene for polycystic kidney disease that encodes an integral membrane proteinT Mochizuki, G Wu, T Hayashi, et al.Human Genetics|July 1, 1987
Human alpha-globin maps to pter-p13.3 in chromosome 16 distal to PGPM H Breuning, K Madan, M Verjaal, et al.Lancet (London, England)|December 14, 1991
Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite markerP C Harris, S Thomas, P J Ratcliffe, et al.JBI Database of Systematic Reviews and Implementation Reports|December 9, 2017
Community-based management of multiple drug resistant tuberculosis in a tertiary hospital in Tanzania: a best practice implementation projectIsaya Jelly, Micah D J PetersPageof 24