Weiffenbach B - Search Results

1

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.

2

A genetic linkage map of human chromosome 5 with 60 RFLP loci.

Weiffenbach B, Falls K, Bricker A, Hall L, McMahon J, Wasmuth J, Funanage V, Donis-Keller H. Weiffenbach B, et al. Genomics. 1991 May;10(1):173-85. doi: 10.1016/0888-7543(91)90498-4. Genomics. 1991. PMID: 1675192

3

A genetic linkage map of the human genome.

Donis-Keller H, Green P, Helms C, Cartinhour S, Weiffenbach B, Stephens K, Keith TP, Bowden DW, Smith DR, Lander ES, et al. Donis-Keller H, et al. Among authors: weiffenbach b. Cell. 1987 Oct 23;51(2):319-37. doi: 10.1016/0092-8674(87)90158-9. Cell. 1987. PMID: 3664638

4

Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD.

Weiffenbach B, Bagley RG, Falls K, Dubois J, Hyser C, Storvick D, Schultz P, Mendell JR, Milner EC, Jacobsen SJ, et al. Weiffenbach B, et al. Mamm Genome. 1992;3(3):143-50. doi: 10.1007/BF00352458. Mamm Genome. 1992. PMID: 1352159

5

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.

6

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

7

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.

8

Single copy probe CRI-L1065 (D6S21) maps to 6cen-6q21.

Weiffenbach B, Trent JM, Frye C, Witkowski C. Weiffenbach B, et al. Nucleic Acids Res. 1991 Jan 11;19(1):199. doi: 10.1093/nar/19.1.199-a. Nucleic Acids Res. 1991. PMID: 1672748 Free PMC article.

9

Dopamine D4 gene 7-repeat allele and attention deficit hyperactivity disorder.

Faraone SV, Biederman J, Weiffenbach B, Keith T, Chu MP, Weaver A, Spencer TJ, Wilens TE, Frazier J, Cleves M, Sakai J. Faraone SV, et al. Among authors: weiffenbach b. Am J Psychiatry. 1999 May;156(5):768-70. doi: 10.1176/ajp.156.5.768. Am J Psychiatry. 1999. PMID: 10327912

10

Cosmid probe CRI-C47 (D4S117) maps to 4p16.1.

Weiffenbach B, Altherr M, Wasmuth JJ. Weiffenbach B, et al. Nucleic Acids Res. 1991 Apr 11;19(7):1728. Nucleic Acids Res. 1991. PMID: 1674148 Free PMC article. No abstract available.

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