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L C Tsui

Showing results (81-90 of 285) with videos related to

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American Journal of Medical Genetics|May 31, 1996
No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian familiesC L Barr, K G Wigg, E Zovko, et al.
Molecular and Cellular Biology|May 29, 2000
Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instabilityA Hellman, A Rahat, S W Scherer, et al.
Genomics|November 1, 1993
Refined mapping of the GM2 activator protein (GM2A) locus to 5q31.3-q33.1, distal to the spinal muscular atrophy locusH H Heng, B Xie, X M Shi, et al.
Developmental Biology|January 1, 1987
Differential regulation of gamma-crystallin genes during mouse lens developmentM Murer-Orlando, R C Paterson, S Lok, et al.
Genomics|September 23, 1997
The human metabotropic glutamate receptor 8 (GRM8) gene: a disproportionately large gene located at 7q31.3-q32.1S W Scherer, S Soder, R M Duvoisin, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1997
Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to chromosome 6M A Crackower, H H Heng, X Shi, et al.
Genetical Research|February 1, 1988
The murine cataractogenic mutation, Cat Fraser, segregates independently of the gamma crystallin genesJ L Rupert, M Kuliszewki, L C Tsui, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Localization of the human gene encoding the 13.3-kDa subunit of mitochondrial complex III (UQCRB) to 8q22 by in situ hybridizationS Malaney, H H Heng, L C Tsui, et al.
Progress in Clinical and Biological Research|January 1, 1987
Utilization of cultured epithelial cells from the sweat gland in studies of the CF defectJ Riordan, J Burns, L C Tsui, et al.
Nucleic Acids Research|January 25, 1989
A rare PvuII RFLP at the CRYB1 locus (17q11.2----17q12)D F Barker, P R Fain, E C Wright, et al.
Pageof 29

Showing results (81-90 of 285) with videos related to

Sort By:
Pageof 29
American Journal of Medical Genetics|May 31, 1996
No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian familiesC L Barr, K G Wigg, E Zovko, et al.
Molecular and Cellular Biology|May 29, 2000
Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instabilityA Hellman, A Rahat, S W Scherer, et al.
Genomics|November 1, 1993
Refined mapping of the GM2 activator protein (GM2A) locus to 5q31.3-q33.1, distal to the spinal muscular atrophy locusH H Heng, B Xie, X M Shi, et al.
Developmental Biology|January 1, 1987
Differential regulation of gamma-crystallin genes during mouse lens developmentM Murer-Orlando, R C Paterson, S Lok, et al.
Genomics|September 23, 1997
The human metabotropic glutamate receptor 8 (GRM8) gene: a disproportionately large gene located at 7q31.3-q32.1S W Scherer, S Soder, R M Duvoisin, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1997
Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to chromosome 6M A Crackower, H H Heng, X Shi, et al.
Genetical Research|February 1, 1988
The murine cataractogenic mutation, Cat Fraser, segregates independently of the gamma crystallin genesJ L Rupert, M Kuliszewki, L C Tsui, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Localization of the human gene encoding the 13.3-kDa subunit of mitochondrial complex III (UQCRB) to 8q22 by in situ hybridizationS Malaney, H H Heng, L C Tsui, et al.
Progress in Clinical and Biological Research|January 1, 1987
Utilization of cultured epithelial cells from the sweat gland in studies of the CF defectJ Riordan, J Burns, L C Tsui, et al.
Nucleic Acids Research|January 25, 1989
A rare PvuII RFLP at the CRYB1 locus (17q11.2----17q12)D F Barker, P R Fain, E C Wright, et al.
Pageof 29