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Human Molecular Genetics|January 1, 1996
Mismatch repair defects in human carcinogenesisJ R Eshleman, S D MarkowitzHuman Molecular Genetics|January 1, 1996
Recombination and nondisjunction in humans and fliesK E Koehler, R S Hawley, S Sherman, et al.Human Molecular Genetics|January 1, 1996
Recent advances in understanding of genetic susceptibility to breast cancerM R StrattonHuman Molecular Genetics|September 1, 1996
Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancerG Moslein, D J Tester, N M Lindor, et al.Human Molecular Genetics|September 1, 1996
A 27 base-pair deletion of the anti-müllerian type II receptor gene is the most common cause of the persistent müllerian duct syndromeS Imbeaud, C Belville, L Messika-Zeitoun, et al.Human Molecular Genetics|September 1, 1996
A human homologue of Drosophila minibrain (MNB) is expressed in the neuronal regions affected in Down syndrome and maps to the critical regionJ Guimerá, C Casas, C Pucharcòs, et al.Human Molecular Genetics|September 1, 1996
Role of late replication timing in the silencing of X-linked genesR S Hansen, T K Canfield, A D Fjeld, et al.Human Molecular Genetics|September 1, 1996
Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx geneL Carrel, P A Hunt, H F WillardHuman Molecular Genetics|September 1, 1996
Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31K Isozumi, R DeLong, J Kaplan, et al.Human Molecular Genetics|October 1, 1996
Full genetic rescue of adenosine deaminase-deficient mice through introduction of the human geneA A Migchielsen, M L Breuer, M S Hershfield, et al.Pageof 1,196