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Human Molecular Genetics|August 1, 1993
A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13M J Francis, K E Morrison, L Campbell, et al.
Human Molecular Genetics|May 1, 1997
Reduced penetrance of the Huntington's disease mutationS M McNeil, A Novelletto, J Srinidhi, et al.
Human Molecular Genetics|June 1, 1993
A gene from chromosome 4p16.3 with similarity to a superfamily of transporter proteinsM P Duyao, S A Taylor, A J Buckler, et al.
Nature Genetics|January 1, 1995
A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patientsT G Thompson, C J DiDonato, L R Simard, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the diseaseS T Winokur, U Bengtsson, J Feddersen, et al.
AIDS Research and Human Retroviruses|November 11, 1991
Human chromosome-dependent and -independent pathways for HIV-2 trans-activationC E Hart, M A Westhafer, J C Galphin, et al.
Somatic Cell and Molecular Genetics|September 1, 1991
New DNA markers in the Huntington's disease gene candidate regionC S Lin, M Altherr, G Bates, et al.
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