B. Williams

发表

A physical map and candidate genes in the BRCA1 region on chromosome 17q12–21

E. Fujimoto, B. Ponder, M. Robertson, 1994, Nature Genetics.

The distal region of 11p13 and associated genetic diseases.

C. Junien, G. Saunders, B. Williams, 1991, Genomics.

Characterization of a 500-kb contig spanning the region between c-Ha-Ras and MUC2 on chromosome 11p15.5.

B. Williams, M. Paris, Bryan R. G. Williams, 2000, Genomics.

Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor.

C. Junien, C. Béroud, C. Antignac, 1990, Genomics.

Localization of the human interferon-induced, ds-RNA activated p68 kinase gene (PRKR) to chromosome 2p21-p22.

J. Squire, E. Meurs, N. McMillan, 1993, Genomics.

Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region.

R. Weksberg, B. Williams, I. Teshima, 1990, Genomics.

Sequence, genomic structure, and chromosomal assignment of human DOC-2.

R. White, J. Stevens, H. Albertsen, 1996, Genomics.

Characterization of the gene encoding the 100-kDa form of human 2',5' oligoadenylate synthetase.

A. Hovnanian, B. Williams, D. Rebouillat, 2000, Genomics.

Human p68 kinase exhibits growth suppression in yeast and homology to the translational regulator GCN2.

K. Schappert, E. Meurs, J. Friesen, 1992, The EMBO journal.

Regional localization of the TIMP gene on the human X chromosome

H. Willard, K. Davies, B. Williams, 1989, Human Genetics.

Definition of the limits of the Wilms tumor locus on human chromosome 11p13.

L. Strong, L. Bonetta, D. Compton, 1990, Genomics.

Isolation of a gene (DLG3) encoding a second member of the discs-large family on chromosome 17q12-q21.

R. White, S. Mazoyer, J. Stevens, 1996, Genomics.

Developmental expression of the endogenous TIMP gene and a TIMP-lacZ fusion gene in transgenic mice.

A. Flenniken, B. Williams, B. Williams, 1990, Genes & development.