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JAMA|February 16, 1994
Advances in molecular analysis of fragile X syndromeS T Warren, D L Nelson
Current Opinion in Neurobiology|October 1, 1993
Trinucleotide repeat expansions in neurological diseaseS T Warren, D L Nelson
Human Molecular Genetics|October 1, 1993
High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndromeI K Hornstra, D L Nelson, S T Warren, et al.
Genomics|August 1, 1992
PCR amplification and analysis of yeast artificial chromosomesJ S Sutcliffe, F Zhang, C T Caskey, et al.
Human Molecular Genetics|April 18, 2000
(Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical featuresA M Peier, K L McIlwain, A Kenneson, et al.
Human Molecular Genetics|September 1, 1992
DNA methylation represses FMR-1 transcription in fragile X syndromeJ S Sutcliffe, D L Nelson, F Zhang, et al.
Nature Genetics|January 1, 1993
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndromeH L Hinds, C T Ashley, J S Sutcliffe, et al.
Nature Genetics|November 1, 1995
Evolution of the cryptic FMR1 CGG repeatE E Eichler, C B Kunst, K A Lugenbeel, et al.
Cell|August 23, 1991
Absence of expression of the FMR-1 gene in fragile X syndromeM Pieretti, F P Zhang, Y H Fu, et al.
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