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P R Cooper

Showing results (131-140 of 135) with videos related to

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Genome Research|February 21, 1998

Contig maps and genomic sequencing identify candidate genes in the usher 1C locusM 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 regionL H Reid, C Davies, P R Cooper, et al.

Genomics|May 8, 1998

Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domainP R Cooper, N J Smilinich, C D Day, et al.

Cell|May 20, 1998

Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndromeR Varon, C Vissinga, M Platzer, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeN J Smilinich, C D Day, G V Fitzpatrick, et al.

Pageof 14

Search research articles

Showing results (131-140 of 135) with videos related to

Sort By:

Pageof 14

You have reached the last page of results.This site can display upto 135 results.

Genome Research|February 21, 1998

Contig maps and genomic sequencing identify candidate genes in the usher 1C locusM 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 regionL H Reid, C Davies, P R Cooper, et al.

Genomics|May 8, 1998

Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domainP R Cooper, N J Smilinich, C D Day, et al.

Cell|May 20, 1998

Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndromeR Varon, C Vissinga, M Platzer, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeN J Smilinich, C D Day, G V Fitzpatrick, et al.

Pageof 14