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The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomasB T Teh, F Farnebo, U Kristoffersson, et al.British Journal of Haematology|February 1, 1990
CD30-positive large cell lymphomas ('Ki-1 lymphoma') are associated with a chromosomal translocation involving 5q35D Y Mason, C Bastard, R Rimokh, et al.Genes, Chromosomes & Cancer|July 1, 1996
Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer familiesC Petersson, N Pandis, F Mertens, et al.Leukemia|July 1, 1988
A new specific chromosomal rearrangement, t(11;20)(p15;q11), in myeloblastic leukemia with maturationF Mitelman, E L Prigogina, E W Fleischman, et al.American Journal of Human Genetics|May 1, 1997
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancerS Håkansson, O Johannsson, U Johansson, et al.Human Molecular Genetics|February 7, 2001
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer familiesJ Vallon-Christersson, C Cayanan, K Haraldsson, et al.Journal of Medical Genetics|November 10, 2000
Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in manM Bugge, G Bruun-Petersen, K Brøndum-Nielsen, et al.Molecular Human Reproduction|January 3, 2001
Identification of human candidate genes for male infertility by digital differential displayC Olesen, C Hansen, E Bendsen, et al.European Journal of Neurology|May 2, 2013
Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?H Lövkvist, M Sjögren, P Höglund, et al.Human Mutation|January 1, 1997
Frequency of RET mutations in long- and short-segment Hirschsprung diseaseM Seri, L Yin, V Barone, et al.Pageof 11