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Items: 1 to 20 of 110

1.

Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease.

Zouali H, Chamaillard M, Lesage S, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, Montague S, Gassull M, Christensen S, Finkel Y, Gower-Rousseau C, Modigliani R, Macry J, Selinger-Leneman H, Thomas G, Hugot JP; GETAID.

Eur J Hum Genet. 2001 Oct;9(10):731-42.

2.
3.

A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder.

Evans KL, Le Hellard S, Morris SW, Lawson D, Whitton C, Semple CA, Fantes JA, Torrance HS, Malloy MP, Maule JC, Humphray SJ, Ross MT, Bentley DR, Muir WJ, Blackwood DH, Porteous DJ.

Genomics. 2001 Feb 1;71(3):315-23.

PMID:
11170748
4.

Peaks of linkage are localized by a BAC/PAC contig of the 6p reading disability locus.

Ahn J, Won TW, Zia A, Reutter H, Kaplan DE, Sparks R, Gruen JR.

Genomics. 2001 Nov;78(1-2):19-29.

PMID:
11707069
5.

Association of NOD2 with Crohn's disease in a homogenous Irish population.

Bairead E, Harmon DL, Curtis AM, Kelly Y, O'Leary C, Gardner M, Leahy DT, Vaughan P, Keegan D, O'Morain C, O'Donoghue D, Shanahan F, Parfrey NA, Quane KA.

Eur J Hum Genet. 2003 Mar;11(3):237-44.

6.

A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium.

Machado RD, Pauciulo MW, Fretwell N, Veal C, Thomson JR, Vilariño Güell C, Aldred M, Brannon CA, Trembath RC, Nichols WC.

Genomics. 2000 Sep 1;68(2):220-8.

PMID:
10964520
7.

Fine mapping of the IBD1 locus did not identify Crohn disease-associated NOD2 variants: implications for complex disease genetics.

van Heel DA, McGovern DP, Cardon LR, Dechairo BM, Lench NJ, Carey AH, Jewell DP.

Am J Med Genet. 2002 Aug 15;111(3):253-9.

PMID:
12210321
8.

Genetic refinement and physical mapping of a 2.3 Mb probable disease region associated with a bipolar affective disorder susceptibility locus on chromosome 4q35.

Badenhop RF, Moses MJ, Scimone A, Adams LJ, Kwok JB, Jones AM, Davison G, Evans MR, Kirkby KC, Hewitt JE, Donald JA, Mitchell PB, Schofield PR.

Am J Med Genet B Neuropsychiatr Genet. 2003 Feb;117B(1):23-32.

PMID:
12555231
9.

Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis. On behalf of the GISC.

Forabosco P, Collins A, Latiano A, Annese V, Clementi M, Andriulli A, Fortina P, Devoto M, Morton NE.

Eur J Hum Genet. 2000 Nov;8(11):846-52.

10.

The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants.

van Heel DA, Dechairo BM, Dawson G, McGovern DP, Negoro K, Carey AH, Cardon LR, Mackay I, Jewell DP, Lench NJ.

Hum Mol Genet. 2003 Oct 15;12(20):2569-75. Epub 2003 Aug 19.

PMID:
12928481
11.

Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC study.

Annese V, Latiano A, Bovio P, Forabosco P, Piepoli A, Lombardi G, Andreoli A, Astegiano M, Gionchetti P, Riegler G, Sturniolo GC, Clementi M, Rappaport E, Fortina P, Devoto M, Gasparini P, Andriulli A.

Eur J Hum Genet. 1999 Jul;7(5):567-73.

12.

A high-resolution 6.0-megabase transcript map of the type 2 diabetes susceptibility region on human chromosome 20.

Fossey SC, Mychaleckyj JC, Pendleton JK, Snyder JR, Bensen JT, Hirakawa S, Rich SS, Freedman BI, Bowden DW.

Genomics. 2001 Aug;76(1-3):45-57.

PMID:
11549316
13.

A BAC contig map over the proximal approximately 3.3 Mb region of horse chromosome 21.

Brinkmeyer-Langford C, Raudsepp T, Gustafson-Seabury A, Chowdhary BP.

Cytogenet Genome Res. 2008;120(1-2):164-72. doi: 10.1159/000118758. Epub 2008 Apr 30.

PMID:
18467843
14.

Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.

Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.

Br J Dermatol. 2005 Jan;152(1):29-36.

PMID:
15656797
15.

Integrated physical map of the human essential tremor gene region (ETM2) on chromosome 2p24.3-p24.2.

Higgins JJ, Lombardi RQ, Pucilowska J, Ruszczyk MU.

Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):128-30.

PMID:
15108195
16.

An integrated map of human 6q22.3-q24 including a 3-Mb high-resolution BAC/PAC contig encompassing a QTL for fetal hemoglobin.

Game L, Close J, Stephens P, Mitchell J, Best S, Rochette J, Louis-dit-Sully C, Riley J, See CG, Sanseau P, Kearney L, Bethel G, Humphray S, Dunham I, Mungall A, Thein SL.

Genomics. 2000 Mar 15;64(3):264-76.

PMID:
10756094
17.

Physical mapping of the rippling muscle disease locus.

Stephan DA, Hoffman EP.

Genomics. 1999 Feb 1;55(3):268-74.

PMID:
10049580
18.

Fine mapping chromosome 16q12 in a collection of 231 systemic lupus erythematosus sibpair and multiplex families.

Gillett CD, Langefeld CD, Williams AH, Ortmann WA, Graham RR, Rodine PR, Selby SA, Gaffney PM, Behrens TW, Moser KL.

Genes Immun. 2005 Feb;6(1):19-23.

PMID:
15538391
19.

[Susceptibility gene of systemic lupus erythematosus in 16q12 in Chinese cohort].

Feng XB, Shen N, Chen SL, Qian J, Wu H, Bao CD, Wang Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Feb;20(1):27-30. Chinese.

PMID:
12579495
20.

A 1.5-Mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11.

Lamartine J, Pitaval A, Soularue P, Lanneluc I, Lemaître G, Kibar Z, Rouleau GA, Waksman G.

Genomics. 2000 Jul 15;67(2):232-6.

PMID:
10903849

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