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Journal of Medical Genetics|November 1, 1989
Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease geneJ Theilmann, S Kanani, R Shiang, et al.Genomics|January 1, 1989
Mapping of the human complement factor I gene to 4q25R Shiang, J C Murray, C C Morton, et al.Cell|July 29, 1994
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasiaR Shiang, L M Thompson, Y Z Zhu, et al.Annals of Neurology|July 1, 1995
Mutational analysis of familial and sporadic hyperekplexiaR Shiang, S G Ryan, Y Z Zhu, et al.Archives of Neurology|June 1, 1995
Molecular genetic reevaluation of the Dutch hyperekplexia familyM A Tijssen, R Shiang, J van Deutekom, et al.American Journal of Human Genetics|March 1, 1988
Pairwise linkage analysis of 11 loci on human chromosome 4J C Murray, K H Buetow, M Smith, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 1, 1997
Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the PhilippinesA C Lidral, J C Murray, K H Buetow, et al.American Journal of Human Genetics|December 1, 1992
Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5qS G Ryan, M J Dixon, M A Nigro, et al.American Journal of Human Genetics|May 1, 1991
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination ratesK H Buetow, R Shiang, P Yang, et al.Genomics|May 1, 1993
The CEPH consortium linkage map of human chromosome 13A M Bowcock, S C Gerken, R I Barnes, et al.Pageof 3