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Nature Genetics|April 1, 1992
Automated DNA sequencing and analysis of 106 kilobases from human chromosome 19q13.3A Martin-Gallardo, W R McCombie, J D Gocayne, et al.Nature Genetics|April 1, 1992
Cretinism with combined hormone deficiency caused by a mutation in the PIT1 geneK Tatsumi, K Miyai, T Notomi, et al.Nature Genetics|May 1, 1992
Construction of a mouse yeast artificial chromosome library in a recombination-deficient strain of yeastF L Chartier, J T Keer, M J Sutcliffe, et al.Nature Genetics|May 1, 1992
Rescue of erythroid development in gene targeted GATA-1- mouse embryonic stem cellsM C Simon, L Pevny, M V Wiles, et al.Nature Genetics|July 1, 1992
Defective colour vision associated with a missense mutation in the human green visual pigment geneJ Winderickx, E Sanocki, D T Lindsey, et al.Nature Genetics|July 1, 1992
Evidence of founder chromosomes in fragile X syndromeR I Richards, K Holman, K Friend, et al.Nature Genetics|August 1, 1992
Kallmann syndrome due to a translocation resulting in an X/Y fusion geneS Guioli, B Incerti, E Zanaria, et al.Nature Genetics|August 1, 1992
Adenovirus-mediated in vivo gene transfer and expression in normal rat liverH A Jaffe, C Danel, G Longenecker, et al.Nature Genetics|June 1, 1992
Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxisB V Nusgens, C Verellen-Dumoulin, T Hermanns-Lê, et al.Nature Genetics|June 1, 1992
Light is a dominant mouse mutation resulting in premature cell deathR Johnson, I J JacksonPageof 737