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S Sparkes

Showing results (221-230 of 276) with videos related to

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American Journal of Medical Genetics|November 1, 1987
Deletion (13)(q14.1q14.3) in two generations: variability of ocular manifestations and definition of the phenotypeW G Wilson, P A Campochiaro, B P Conway, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1983
Genetic linkage studies with cleft lip and palate: report of two family studiesM A Spence, L Glass, B F Crandall, et al.
Genes, Chromosomes & Cancer|July 9, 1999
Linkage analysis and loss of heterozygosity for chromosome arm 1p in familial breast cancerR C Millikan, S A Ingles, A T Diep, et al.
American Journal of Human Genetics|February 1, 1996
Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosaT L Kojis, C Heinzmann, P Flodman, et al.
Epilepsia|January 1, 1989
Mapping the gene for juvenile myoclonic epilepsyA V Delgado-Escueta, D A Greenberg, L Treiman, et al.
Molecular Vision|April 4, 1998
Regional mapping of the human MP70 (Cx50; connexin 50) gene by fluorescence in situ hybridization to 1q21.1D D Geyer, R L Church, E C Steele, et al.
Epilepsia|January 1, 1994
Progress in mapping human epilepsy genesA V Delgado-Escueta, J M Serratosa, A Liu, et al.
Blood|September 1, 1989
CML-T1: a cell line derived from T-lymphocyte acute phase of chronic myelogenous leukemiaK Kuriyama, R P Gale, M Tomonaga, et al.
The Journal of Biological Chemistry|November 25, 1987
The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationshipsD A Sweetser, E H Birkenmeier, I J Klisak, et al.
Genomics|January 1, 1992
Assignment of the gene (RLBP1) for cellular retinaldehyde-binding protein (CRALBP) to human chromosome 15q26 and mouse chromosome 7R S Sparkes, C Heinzmann, S Goldflam, et al.
Pageof 28

Showing results (221-230 of 276) with videos related to

Sort By:
Pageof 28
American Journal of Medical Genetics|November 1, 1987
Deletion (13)(q14.1q14.3) in two generations: variability of ocular manifestations and definition of the phenotypeW G Wilson, P A Campochiaro, B P Conway, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1983
Genetic linkage studies with cleft lip and palate: report of two family studiesM A Spence, L Glass, B F Crandall, et al.
Genes, Chromosomes & Cancer|July 9, 1999
Linkage analysis and loss of heterozygosity for chromosome arm 1p in familial breast cancerR C Millikan, S A Ingles, A T Diep, et al.
American Journal of Human Genetics|February 1, 1996
Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosaT L Kojis, C Heinzmann, P Flodman, et al.
Epilepsia|January 1, 1989
Mapping the gene for juvenile myoclonic epilepsyA V Delgado-Escueta, D A Greenberg, L Treiman, et al.
Molecular Vision|April 4, 1998
Regional mapping of the human MP70 (Cx50; connexin 50) gene by fluorescence in situ hybridization to 1q21.1D D Geyer, R L Church, E C Steele, et al.
Epilepsia|January 1, 1994
Progress in mapping human epilepsy genesA V Delgado-Escueta, J M Serratosa, A Liu, et al.
Blood|September 1, 1989
CML-T1: a cell line derived from T-lymphocyte acute phase of chronic myelogenous leukemiaK Kuriyama, R P Gale, M Tomonaga, et al.
The Journal of Biological Chemistry|November 25, 1987
The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationshipsD A Sweetser, E H Birkenmeier, I J Klisak, et al.
Genomics|January 1, 1992
Assignment of the gene (RLBP1) for cellular retinaldehyde-binding protein (CRALBP) to human chromosome 15q26 and mouse chromosome 7R S Sparkes, C Heinzmann, S Goldflam, et al.
Pageof 28