Harris PC - Search Results

1

De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16).

Lamb J, Harris PC, Wilkie AO, Wood WG, Dauwerse JG, Higgs DR. Lamb J, et al. Among authors: harris pc. Am J Hum Genet. 1993 Apr;52(4):668-76. Am J Hum Genet. 1993. PMID: 8460633 Free PMC article.

2

Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16.

Wilkie AO, Higgs DR, Rack KA, Buckle VJ, Spurr NK, Fischel-Ghodsian N, Ceccherini I, Brown WR, Harris PC. Wilkie AO, et al. Among authors: harris pc. Cell. 1991 Feb 8;64(3):595-606. doi: 10.1016/0092-8674(91)90243-r. Cell. 1991. PMID: 1991321

3

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

Wilkie AO, Buckle VJ, Harris PC, Lamb J, Barton NJ, Reeders ST, Lindenbaum RH, Nicholls RD, Barrow M, Bethlenfalvay NC, et al. Wilkie AO, et al. Among authors: harris pc. Am J Hum Genet. 1990 Jun;46(6):1112-26. Am J Hum Genet. 1990. PMID: 2339704 Free PMC article.

4

A long-range restriction map between the alpha-globin complex and a marker closely linked to the polycystic kidney disease 1 (PKD1) locus.

Harris PC, Barton NJ, Higgs DR, Reeders ST, Wilkie AO. Harris PC, et al. Genomics. 1990 Jun;7(2):195-206. doi: 10.1016/0888-7543(90)90541-2. Genomics. 1990. PMID: 2347584

5

Structure of the human 3-methyladenine DNA glycosylase gene and localization close to the 16p telomere.

Vickers MA, Vyas P, Harris PC, Simmons DL, Higgs DR. Vickers MA, et al. Among authors: harris pc. Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3437-41. doi: 10.1073/pnas.90.8.3437. Proc Natl Acad Sci U S A. 1993. PMID: 8475094 Free PMC article.

6

A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)n.

Wilkie AO, Lamb J, Harris PC, Finney RD, Higgs DR. Wilkie AO, et al. Among authors: harris pc. Nature. 1990 Aug 30;346(6287):868-71. doi: 10.1038/346868a0. Nature. 1990. PMID: 1975428

7

Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16.

Germino GG, Barton NJ, Lamb J, Higgs DR, Harris P, Xiao GH, Scherer G, Nakamura Y, Reeders ST. Germino GG, et al. Am J Hum Genet. 1990 May;46(5):925-33. Am J Hum Genet. 1990. PMID: 2339691 Free PMC article.

8

Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease.

Lamb J, Wilkie AO, Harris PC, Buckle VJ, Lindenbaum RH, Barton NJ, Reeders ST, Weatherall DJ, Higgs DR. Lamb J, et al. Among authors: harris pc. Lancet. 1989 Oct 7;2(8667):819-24. doi: 10.1016/s0140-6736(89)92995-4. Lancet. 1989. PMID: 2477654

9

A human PKD1 transgene generates functional polycystin-1 in mice and is associated with a cystic phenotype.

Pritchard L, Sloane-Stanley JA, Sharpe JA, Aspinwall R, Lu W, Buckle V, Strmecki L, Walker D, Ward CJ, Alpers CE, Zhou J, Wood WG, Harris PC. Pritchard L, et al. Among authors: harris pc. Hum Mol Genet. 2000 Nov 1;9(18):2617-27. doi: 10.1093/hmg/9.18.2617. Hum Mol Genet. 2000. PMID: 11063721

10

Characterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysis.

Rack KA, Harris PC, MacCarthy AB, Boone R, Raynham H, McKinley M, Fitchett M, Towe CM, Rudd P, Armour JA, et al. Rack KA, et al. Among authors: harris pc. Am J Hum Genet. 1993 May;52(5):987-97. Am J Hum Genet. 1993. PMID: 8488848 Free PMC article.

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