Weiffenbach B - Search Results

1

Frequency of the variant allele CYP2D6(C) among North American Caucasian lung cancer patients and controls.

Shaw GL, Weiffenbach B, Falk RT, Frame JN, Issaq HJ, Moir DT, Caporaso N. Shaw GL, et al. Among authors: weiffenbach b. Lung Cancer. 1997 May;17(1):61-8. doi: 10.1016/s0169-5002(97)00649-1. Lung Cancer. 1997. PMID: 9194027

2

Genetic polymorphism of CYP2D6 and lung cancer risk.

Shaw GL, Falk RT, Frame JN, Weiffenbach B, Nesbitt JC, Pass HI, Caporaso NE, Moir DT, Tucker MA. Shaw GL, et al. Among authors: weiffenbach b. Cancer Epidemiol Biomarkers Prev. 1998 Mar;7(3):215-9. Cancer Epidemiol Biomarkers Prev. 1998. PMID: 9521436

3

Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype.

Saxena R, Shaw GL, Relling MV, Frame JN, Moir DT, Evans WE, Caporaso N, Weiffenbach B. Saxena R, et al. Among authors: weiffenbach b. Hum Mol Genet. 1994 Jun;3(6):923-6. doi: 10.1093/hmg/3.6.923. Hum Mol Genet. 1994. PMID: 7951238 Clinical Trial.

4

Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35.

Weiffenbach B, Bagley R, Falls K, Hyser C, Storvick D, Jacobsen SJ, Schultz P, Mendell J, Willems van Dijk K, Milner EC, et al. Weiffenbach B, et al. Am J Hum Genet. 1992 Aug;51(2):416-23. Am J Hum Genet. 1992. PMID: 1642240 Free PMC article.

5

Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination events.

Weiffenbach B, Dubois J, Storvick D, Tawil R, Jacobsen SJ, Gilbert J, Wijmenga C, Mendell JR, Winokur S, Altherr MR, et al. Weiffenbach B, et al. Nat Genet. 1993 Jun;4(2):165-9. doi: 10.1038/ng0693-165. Nat Genet. 1993. PMID: 8102297

6

YAC contigs for 4q35 in the region of the facioscapulohumeral muscular dystrophy (FSHD) gene.

Weiffenbach B, Dubois J, Manning S, Ma NS, Schutte BC, Winokur ST, Altherr MR, Jacobsen SJ, Stanton VP Jr, Yokoyama K, et al. Weiffenbach B, et al. Genomics. 1994 Feb;19(3):532-41. doi: 10.1006/geno.1994.1103. Genomics. 1994. PMID: 8188296

7

Homothallic mating type switching generates lethal chromosome breaks in rad52 strains of Saccharomyces cerevisiae.

Weiffenbach B, Haber JE. Weiffenbach B, et al. Mol Cell Biol. 1981 Jun;1(6):522-34. doi: 10.1128/mcb.1.6.522-534.1981. Mol Cell Biol. 1981. PMID: 6765605 Free PMC article.

8

Construction of a linkage map of the human genome, and its application to mapping genetic diseases.

Green P, Helms C, Weiffenbach B, Stephens K, Keith T, Bowden D, Smith D, Donis-Keller H. Green P, et al. Among authors: weiffenbach b. Clin Chem. 1989 Jul;35(7 Suppl):B33-7. Clin Chem. 1989. PMID: 2568196 Review.

9

Report of the second international workshop on human chromosome 5 mapping: consensus genetic map.

Plaetke R, Weber J, Wood S, Dean M, Jeffreys AJ, Weiffenbach B, Vergnaud G, Vogelstein B, White R. Plaetke R, et al. Among authors: weiffenbach b. Cytogenet Cell Genet. 1992;61(4):237-42. Cytogenet Cell Genet. 1992. PMID: 1362533 No abstract available.

10

A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).

Winokur ST, Schutte B, Weiffenbach B, Washington SS, McElligott D, Chakravarti A, Wasmuth JH, Altherr MR. Winokur ST, et al. Among authors: weiffenbach b. Am J Hum Genet. 1993 Oct;53(4):874-80. Am J Hum Genet. 1993. PMID: 8213815 Free PMC article.

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