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Genomics
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May 20, 1999
Bestrophin gene mutations in patients with Best vitelliform macular dystrophy
G M Caldwell, L E Kakuk, I B Griesinger, et al.
Cytogenetics and Cell Genetics
|
April 18, 2001
Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1-->p14
G M Caldwell, R L Eddy, C D Day, et al.
Genome Research
|
February 21, 1998
Contig maps and genomic sequencing identify candidate genes in the usher 1C locus
M J Higgins, C D Day, N J Smilinich, et al.
Genomics
|
August 1, 1997
A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region
L H Reid, C Davies, P R Cooper, et al.
Genomics
|
December 1, 1996
A 1.5-megabase physical map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13
T F Wood, E S Srivatsan, R Chakrabarti, et al.
Nature Genetics
|
March 21, 1998
Linkage-disequilibrium mapping without genotyping
V G Cheung, J P Gregg, K J Gogolin-Ewens, et al.
Genomics
|
April 15, 1996
A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23
K Savitsky, Y Ziv, A Bar-Shira, et al.
Biology of Reproduction
|
July 25, 2000
Spermatid-specific expression of the novel X-linked gene product SPAN-X localized to the nucleus of human spermatozoa
V A Westbrook, A B Diekman, K L Klotz, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 2, 1996
A high-resolution physical map of human chromosome 11
S Qin, N J Nowak, J Zhang, et al.
Genomics
|
May 8, 1998
Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain
P R Cooper, N J Smilinich, C D Day, et al.
Page
of 30
Search research articles
Search
Showing results (281-290 of 295) with videos related to
Sort By:
Page
of 30
Genomics
|
May 20, 1999
Bestrophin gene mutations in patients with Best vitelliform macular dystrophy
G M Caldwell, L E Kakuk, I B Griesinger, et al.
Cytogenetics and Cell Genetics
|
April 18, 2001
Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1-->p14
G M Caldwell, R L Eddy, C D Day, et al.
Genome Research
|
February 21, 1998
Contig maps and genomic sequencing identify candidate genes in the usher 1C locus
M J Higgins, C D Day, N J Smilinich, et al.
Genomics
|
August 1, 1997
A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region
L H Reid, C Davies, P R Cooper, et al.
Genomics
|
December 1, 1996
A 1.5-megabase physical map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13
T F Wood, E S Srivatsan, R Chakrabarti, et al.
Nature Genetics
|
March 21, 1998
Linkage-disequilibrium mapping without genotyping
V G Cheung, J P Gregg, K J Gogolin-Ewens, et al.
Genomics
|
April 15, 1996
A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23
K Savitsky, Y Ziv, A Bar-Shira, et al.
Biology of Reproduction
|
July 25, 2000
Spermatid-specific expression of the novel X-linked gene product SPAN-X localized to the nucleus of human spermatozoa
V A Westbrook, A B Diekman, K L Klotz, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 2, 1996
A high-resolution physical map of human chromosome 11
S Qin, N J Nowak, J Zhang, et al.
Genomics
|
May 8, 1998
Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain
P R Cooper, N J Smilinich, C D Day, et al.
Page
of 30