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Human Molecular Genetics|February 28, 1998
Emerin deletions occurring on both Xq28 inversion backgroundsK Small, S T WarrenNature Genetics|May 1, 1997
Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeatsK Small, J Iber, S T WarrenMammalian Genome : Official Journal of the International Mammalian Genome Society|May 1, 1997
Isolation and characterization of the complete mouse emerin geneK Small, M Wagener, S T WarrenThe Journal of Biological Chemistry|June 23, 1998
Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation proteinV Brown, K Small, L Lakkis, et al.American Journal of Medical Genetics|May 1, 1988
Fragile X syndrome: a hypothesis regarding the molecular mechanism of the phenotypeS T WarrenHuman Molecular Genetics|October 1, 1995
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the diseaseS Bione, K Small, V M Aksmanovic, et al.Journal of Neuroscience Research|January 1, 1985
Membrane specializations of neuritic growth cones in vivo: a quantitative IMP analysisR K SmallSeminars in Reproductive Medicine|August 2, 2001
The female and the fragile X reviewedA Kenneson, S T WarrenHuman Molecular Genetics|April 18, 2000
Understanding the molecular basis of fragile X syndromeP Jin, S T WarrenPageof 20