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Science (New York, N.Y.)|June 24, 1994
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesisJ K Nancarrow, E Kremer, K Holman, et al.Science (New York, N.Y.)|June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)nE J Kremer, M Pritchard, M Lynch, et al.Molecular Cell|July 14, 1998
FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesisD R Hewett, O Handt, L Hobson, et al.Human Genetics|September 15, 2000
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHMK L Friend, D Crimmins, T G Phan, et al.Journal of Medical Genetics|June 1, 1992
Experience with direct molecular diagnosis of fragile XJ C Mulley, S Yu, A K Gedeon, et al.Nature|October 28, 1982
Human metallothionein genes--primary structure of the metallothionein-II gene and a related processed geneM Karin, R I RichardsJournal of Medical Genetics|December 1, 1991
Determination of Duchenne muscular dystrophy carrier status by single strand conformation polymorphism analysis of deleted regions of the dystrophin locusR I Richards, K FriendEnvironmental Health Perspectives|March 1, 1984
The human metallothionein gene family: structure and expressionM Karin, R I RichardsNucleic Acids Research|May 25, 1982
Human metallothionein genes: molecular cloning and sequence analysis of the mRNAM Karin, R I RichardsPageof 57