Frischauf AM - Search Results

1

Comparative genome analysis delimits a chromosomal domain and identifies key regulatory elements in the alpha globin cluster.

Flint J, Tufarelli C, Peden J, Clark K, Daniels RJ, Hardison R, Miller W, Philipsen S, Tan-Un KC, McMorrow T, Frampton J, Alter BP, Frischauf AM, Higgs DR. Flint J, et al. Among authors: frischauf am. Hum Mol Genet. 2001 Feb 15;10(4):371-82. doi: 10.1093/hmg/10.4.371. Hum Mol Genet. 2001. PMID: 11157800

2

Characterization of a widely expressed gene (LUC7-LIKE; LUC7L) defining the centromeric boundary of the human alpha-globin domain.

Tufarelli C, Frischauf AM, Hardison R, Flint J, Higgs DR. Tufarelli C, et al. Among authors: frischauf am. Genomics. 2001 Feb 1;71(3):307-14. doi: 10.1006/geno.2000.6394. Genomics. 2001. PMID: 11170747

3

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: frischauf am. Hum Mol Genet. 1993 Aug;2(8):1161-7. doi: 10.1093/hmg/2.8.1161. Hum Mol Genet. 1993. PMID: 8401497

4

Germline mutations of the CDKN2 gene in UK melanoma families.

Harland M, Meloni R, Gruis N, Pinney E, Brookes S, Spurr NK, Frischauf AM, Bataille V, Peters G, Cuzick J, Selby P, Bishop DT, Bishop JN. Harland M, et al. Among authors: frischauf am. Hum Mol Genet. 1997 Nov;6(12):2061-7. doi: 10.1093/hmg/6.12.2061. Hum Mol Genet. 1997. PMID: 9328469

5

Haplotype analysis in autosomal dominant polycystic kidney disease.

Pound SE, Thomas S, Snarey A, Macnicol AM, Watson ML, Pignatelli PM, Frischauf AM, Harris PC, Wright AF. Pound SE, et al. Among authors: frischauf am. J Med Genet. 1995 Mar;32(3):208-12. doi: 10.1136/jmg.32.3.208. J Med Genet. 1995. PMID: 7783171 Free PMC article.

6

Genetic heterogeneity in familial malignant melanoma.

MacGeoch C, Bishop JA, Bataille V, Bishop DT, Frischauf AM, Meloni R, Cuzick J, Pinney E, Spurr NK. MacGeoch C, et al. Among authors: frischauf am. Hum Mol Genet. 1994 Dec;3(12):2195-200. doi: 10.1093/hmg/3.12.2195. Hum Mol Genet. 1994. PMID: 7881419

7

Positional cloning uncovers a new old oncogene.

Frischauf AM. Frischauf AM. Hum Mol Genet. 1993 Jul;2(7):847-8. doi: 10.1093/hmg/2.7.847. Hum Mol Genet. 1993. PMID: 8103402 Review. No abstract available.

8

A high-resolution radiation hybrid map of the region surrounding the Gorlin syndrome gene.

Obermayr F, Walter MA, Jones HB, Goodfellow PN, Frischauf AM. Obermayr F, et al. Among authors: frischauf am. Eur J Hum Genet. 1996;4(4):242-5. doi: 10.1159/000472206. Eur J Hum Genet. 1996. PMID: 8875192

9

The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome.

Ellis NA, Goodfellow PJ, Pym B, Smith M, Palmer M, Frischauf AM, Goodfellow PN. Ellis NA, et al. Among authors: frischauf am. Nature. 1989 Jan 5;337(6202):81-4. doi: 10.1038/337081a0. Nature. 1989. PMID: 2909893

10

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: frischauf am. Mol Cell Probes. 1992 Dec;6(6):513-20. doi: 10.1016/0890-8508(92)90048-3. Mol Cell Probes. 1992. PMID: 1480191

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