E W Jabs - JoVE Visualize

Showing results (41-50 of 103) with videos related to

Pageof 11

Sort By:

Cytogenetics and Cell Genetics|February 22, 2002

Fibroblast growth factor receptor 2 (FGFR2): genomic sequence and variationsR G Ingersoll, W A Paznekas, A K Tran, et al.

Genomics|October 1, 1992

Chromosomal assignment of a gene encoding a new collagen type (COL15A1) to 9q21 --> q22K Huebner, L A Cannizzaro, E W Jabs, et al.

Cytogenetics and Cell Genetics|January 1, 1993

Cytogenetic survey in systemic sclerosis: correlation of aneuploidy with the presence of anticentromere antibodiesE W Jabs, C M Tuck-Muller, G J Anhalt, et al.

Gene|January 30, 1993

Human cDNA clones transcribed from an unusually high-molecular-weight RNA encode a new collagen chainJ C Myers, M J Sun, J A D'Ippolito, et al.

Genomics|March 1, 1991

A centromere-based genetic map of the short arm of human chromosome 6H Blanché, H Y Zoghbi, E W Jabs, et al.

American Journal of Human Genetics|June 1, 1986

Regional localization of DNA sequences on chromosome 21 using somatic cell hybridsM L Van Keuren, P C Watkins, H A Drabkin, et al.

American Journal of Diseases of Children (1960)|December 1, 1993

Cytogenetic survey of Apert syndrome. Reevaluation of a translocation (2;9)(p11.2;q34.2) in a patient suggests the breakpoints are not related to the disorderA F Lewanda, M M Cohen, J Hood, et al.

Human Mutation|July 29, 1999

Clinical spectrum of fibroblast growth factor receptor mutationsM R Passos-Bueno, W R Wilcox, E W Jabs, et al.

Biochemical and Biophysical Research Communications|October 10, 1992

Structure of the human spermidine/spermine N1-acetyltransferase gene (exon/intron gene organization and localization to Xp22.1)L Xiao, P Celano, A R Mank, et al.

Genomics|January 1, 1991

Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to bothE W Jabs, A C Warren, E W Taylor, et al.

Pageof 11

Showing results (41-50 of 103) with videos related to

Sort By:

Pageof 11

Cytogenetics and Cell Genetics|February 22, 2002

Fibroblast growth factor receptor 2 (FGFR2): genomic sequence and variationsR G Ingersoll, W A Paznekas, A K Tran, et al.

Genomics|October 1, 1992

Chromosomal assignment of a gene encoding a new collagen type (COL15A1) to 9q21 --> q22K Huebner, L A Cannizzaro, E W Jabs, et al.

Cytogenetics and Cell Genetics|January 1, 1993

Cytogenetic survey in systemic sclerosis: correlation of aneuploidy with the presence of anticentromere antibodiesE W Jabs, C M Tuck-Muller, G J Anhalt, et al.

Gene|January 30, 1993

Human cDNA clones transcribed from an unusually high-molecular-weight RNA encode a new collagen chainJ C Myers, M J Sun, J A D'Ippolito, et al.

Genomics|March 1, 1991

A centromere-based genetic map of the short arm of human chromosome 6H Blanché, H Y Zoghbi, E W Jabs, et al.

American Journal of Human Genetics|June 1, 1986

Regional localization of DNA sequences on chromosome 21 using somatic cell hybridsM L Van Keuren, P C Watkins, H A Drabkin, et al.

American Journal of Diseases of Children (1960)|December 1, 1993

Cytogenetic survey of Apert syndrome. Reevaluation of a translocation (2;9)(p11.2;q34.2) in a patient suggests the breakpoints are not related to the disorderA F Lewanda, M M Cohen, J Hood, et al.

Human Mutation|July 29, 1999

Clinical spectrum of fibroblast growth factor receptor mutationsM R Passos-Bueno, W R Wilcox, E W Jabs, et al.

Biochemical and Biophysical Research Communications|October 10, 1992

Structure of the human spermidine/spermine N1-acetyltransferase gene (exon/intron gene organization and localization to Xp22.1)L Xiao, P Celano, A R Mank, et al.

Genomics|January 1, 1991

Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to bothE W Jabs, A C Warren, E W Taylor, et al.

Pageof 11