Wasmuth J - Search Results

1

Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4.

Allitto BA, McClatchey AI, Barnes G, Altherr M, Wasmuth J, Frischauf AM, MacDonald ME, Gusella J. Allitto BA, et al. Among authors: wasmuth j. Mol Cell Probes. 1992 Dec;6(6):513-20. doi: 10.1016/0890-8508(92)90048-3. Mol Cell Probes. 1992. PMID: 1480191

2

Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat.

Ambrose CM, Duyao MP, Barnes G, Bates GP, Lin CS, Srinidhi J, Baxendale S, Hummerich H, Lehrach H, Altherr M, Wasmuth J, Buckler A, Church D, Housman D, Berks M, Micklem G, Durbin R, Dodge A, Read A, Gusella J, MacDonald ME. Ambrose CM, et al. Among authors: wasmuth j. Somat Cell Mol Genet. 1994 Jan;20(1):27-38. doi: 10.1007/BF02257483. Somat Cell Mol Genet. 1994. PMID: 8197474

3

Complex patterns of linkage disequilibrium in the Huntington disease region.

MacDonald ME, Lin C, Srinidhi L, Bates G, Altherr M, Whaley WL, Lehrach H, Wasmuth J, Gusella JF. MacDonald ME, et al. Among authors: wasmuth j. Am J Hum Genet. 1991 Oct;49(4):723-34. Am J Hum Genet. 1991. PMID: 1680285 Free PMC article.

4

Identification and characterization of two novel tetratricopeptide repeat-containing genes.

Murthy AE, Bernards A, Church D, Wasmuth J, Gusella JF. Murthy AE, et al. Among authors: wasmuth j. DNA Cell Biol. 1996 Sep;15(9):727-35. doi: 10.1089/dna.1996.15.727. DNA Cell Biol. 1996. PMID: 8836031

5

A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13.

Francis MJ, Morrison KE, Campbell L, Grewal PK, Christodoulou Z, Daniels RJ, Monaco AP, Frischauf AM, McPherson J, Wasmuth J, et al. Francis MJ, et al. Among authors: wasmuth j. Hum Mol Genet. 1993 Aug;2(8):1161-7. doi: 10.1093/hmg/2.8.1161. Hum Mol Genet. 1993. PMID: 8401497

6

Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.

Robbins C, Theilmann J, Youngman S, Haines J, Altherr MJ, Harper PS, Payne C, Junker A, Wasmuth J, Hayden MR. Robbins C, et al. Among authors: wasmuth j. Am J Hum Genet. 1989 Mar;44(3):422-5. Am J Hum Genet. 1989. PMID: 2521771 Free PMC article.

7

Single copy probe CRI-L114 (D4S110) maps to 4p16.1.

Weiffenbach B, Altherr M, Wasmuth J. Weiffenbach B, et al. Among authors: wasmuth j. Nucleic Acids Res. 1991 Apr 11;19(7):1728. Nucleic Acids Res. 1991. PMID: 1674149 Free PMC article. No abstract available.

8

A DNA probe, D5 [D4S90] mapping to human chromosome 4p16.3.

Youngman S, Shaw DJ, Gusella JF, MacDonald M, Stanbridge EJ, Wasmuth J, Harper PS. Youngman S, et al. Among authors: wasmuth j. Nucleic Acids Res. 1988 Feb 25;16(4):1648. doi: 10.1093/nar/16.4.1648. Nucleic Acids Res. 1988. PMID: 2894638 Free PMC article.

9

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: wasmuth jh. Am J Hum Genet. 1993 Oct;53(4):874-80. Am J Hum Genet. 1993. PMID: 8213815 Free PMC article.

10

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. Among authors: wasmuth j. Genomics. 1991 May;10(1):173-85. doi: 10.1016/0888-7543(91)90498-4. Genomics. 1991. PMID: 1675192

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