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Human Molecular Genetics|November 13, 1998
The Treacher Collins syndrome (TCOF1) gene product, treacle, is targeted to the nucleolus by signals in its C-terminusS T Winokur, R ShiangHuman Molecular Genetics|May 1, 1997
Sequence analysis, identification of evolutionary conserved motifs and expression analysis of murine tcof1 provide further evidence for a potential function for the gene and its human homologue, TCOF1J Dixon, K Hovanes, R Shiang, et al.EXS|January 1, 1991
Generation of variability at VNTR loci in human DNAR Wolff, Y Nakamura, S Odelberg, et al.Genome Research|August 1, 1997
A high-resolution physical and transcript map of the Cri du chat region of human chromosome 5pD M Church, J Yang, M Bocian, et al.Human Genetics|July 1, 1987
Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase lociJ C Murray, R Shiang, L R Carlock, et al.Cytogenetics and Cell Genetics|January 1, 1994
Genes encoding adrenergic receptors are not clustered on the long arm of human chromosome 5S K Loftus, R Shiang, J A Warrington, et al.Nature Genetics|December 1, 1993
Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexiaR Shiang, S G Ryan, Y Z Zhu, et al.Cytogenetics and Cell Genetics|January 1, 1991
Chromosomal localization of the human gene for annexin V (placental anticoagulant protein I) to 4q26----q28J F Tait, D A Frankenberry, R Shiang, et al.American Journal of Human Genetics|October 1, 1993
Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO)R Shiang, A C Lidral, H H Ardinger, et al.Clinical Neurology and Neurosurgery|August 1, 1997
Hyperekplexia-like syndromes without mutations in the GLRA1 geneM N Vergouwe, M A Tijssen, R Shiang, et al.Pageof 3