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J B Bateman

Showing results (81-90 of 92) with videos related to

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Investigative Ophthalmology & Visual Science|September 28, 2000
A new betaA1-crystallin splice junction mutation in autosomal dominant cataractJ B Bateman, D D Geyer, P Flodman, 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.
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.
Human Genetics|January 1, 1992
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on XpS Lindsay, D L Thiselton, J B Bateman, et al.
Genomics|March 1, 1992
Assignment of the beta-subunit of rod photoreceptor cGMP phosphodiesterase gene PDEB (homolog of the mouse rd gene) to human chromosome 4p16J B Bateman, I Klisak, T Kojis, et al.
The American Journal of Psychiatry|February 1, 1988
Electroretinograms in autism: a pilot study of b-wave amplitudesE R Ritvo, D Creel, G Realmuto, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
A new locus for autosomal dominant cataract on chromosome 12q13J B Bateman, M Johannes, P Flodman, et al.
Genomics|September 15, 1994
Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphismsC Heinzmann, T L Kojis, P Gonzalez, et al.
Somatic Cell and Molecular Genetics|September 1, 1984
Wilms' tumor-aniridia association: segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin geneJ H Fisher, Y E Miller, R S Sparkes, et al.
Transactions of the American Ophthalmological Society|January 1, 1993
Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locusJ B Bateman, T L Kojis, R M Cantor, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Investigative Ophthalmology & Visual Science|September 28, 2000
A new betaA1-crystallin splice junction mutation in autosomal dominant cataractJ B Bateman, D D Geyer, P Flodman, 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.
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.
Human Genetics|January 1, 1992
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on XpS Lindsay, D L Thiselton, J B Bateman, et al.
Genomics|March 1, 1992
Assignment of the beta-subunit of rod photoreceptor cGMP phosphodiesterase gene PDEB (homolog of the mouse rd gene) to human chromosome 4p16J B Bateman, I Klisak, T Kojis, et al.
The American Journal of Psychiatry|February 1, 1988
Electroretinograms in autism: a pilot study of b-wave amplitudesE R Ritvo, D Creel, G Realmuto, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
A new locus for autosomal dominant cataract on chromosome 12q13J B Bateman, M Johannes, P Flodman, et al.
Genomics|September 15, 1994
Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphismsC Heinzmann, T L Kojis, P Gonzalez, et al.
Somatic Cell and Molecular Genetics|September 1, 1984
Wilms' tumor-aniridia association: segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin geneJ H Fisher, Y E Miller, R S Sparkes, et al.
Transactions of the American Ophthalmological Society|January 1, 1993
Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locusJ B Bateman, T L Kojis, R M Cantor, et al.
Pageof 10