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Items: 1 to 20 of 126

1.

Haplotype and linkage disequilibrium analysis of the CRMP1 and EVC genes.

Sivakumaran TA, Lesperance MM.

Int J Mol Med. 2004 Nov;14(5):903-7.

PMID:
15492864
2.

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM.

Hum Mol Genet. 2001 Oct 15;10(22):2501-8.

PMID:
11709537
3.

Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis.

Ruiz-Perez VL, Ide SE, Strom TM, Lorenz B, Wilson D, Woods K, King L, Francomano C, Freisinger P, Spranger S, Marino B, Dallapiccola B, Wright M, Meitinger T, Polymeropoulos MH, Goodship J.

Nat Genet. 2000 Mar;24(3):283-6. Erratum in: Nat Genet 2000 May;25(1):125.

PMID:
10700184
4.

An isochore transition in the NF1 gene region coincides with a switch in the extent of linkage disequilibrium.

Eisenbarth I, Vogel G, Krone W, Vogel W, Assum G.

Am J Hum Genet. 2000 Oct;67(4):873-80. Epub 2000 Sep 6.

5.

Genetic variations in the WFS1 gene in Japanese with type 2 diabetes and bipolar disorder.

Kawamoto T, Horikawa Y, Tanaka T, Kabe N, Takeda J, Mikuni M.

Mol Genet Metab. 2004 Jul;82(3):238-45.

PMID:
15234338
6.

Complex high-resolution linkage disequilibrium and haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb of sequence on human chromosome 21.

Olivier M, Bustos VI, Levy MR, Smick GA, Moreno I, Bushard JM, Almendras AA, Sheppard K, Zierten DL, Aggarwal A, Carlson CS, Foster BD, Vo N, Kelly L, Liu X, Cox DR.

Genomics. 2001 Nov;78(1-2):64-72.

PMID:
11707074
7.

Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis.

D'Asdia MC, Torrente I, Consoli F, Ferese R, Magliozzi M, Bernardini L, Guida V, Digilio MC, Marino B, Dallapiccola B, De Luca A.

Eur J Med Genet. 2013 Feb;56(2):80-7. doi: 10.1016/j.ejmg.2012.11.005. Epub 2012 Dec 7.

PMID:
23220543
8.

Haplotype frequencies and linkage disequilibrium analysis of four frequent polymorphisms at the PTH/PTH-related peptide receptor gene locus.

Fröhlich LF, Gensure RC, Schipani E, Jüppner H, Bastepe M.

Mol Cell Probes. 2004 Oct;18(5):353-7.

PMID:
15294324
10.

Comparative study of the haplotype structure and linkage disequilibrium of chromosome 1p36.2 region in the Korean and Japanese populations.

Akesaka T, Lee SG, Ohashi J, Bannai M, Tsuchiya N, Yoon Y, Tokunaga K, Song K.

J Hum Genet. 2004;49(11):603-9. Epub 2004 Oct 6.

PMID:
15480877
11.

Patterns of genetic variation in the hypertension candidate gene GRK4: ethnic variation and haplotype structure.

Lohmueller KE, Wong LJ, Mauney MM, Jiang L, Felder RA, Jose PA, Williams SM.

Ann Hum Genet. 2006 Jan;70(Pt 1):27-41.

12.

Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.

Watanabe Y, Murray JC, Bjork BC, Bird CP, Chiang PW, Gregory SG, Kurnit DM, Schutte BC.

Hum Mutat. 2001 Nov;18(5):422-34.

PMID:
11668635
13.

Haplotype frequency distribution and linkage disequilibrium analysis of single nucleotide polymorphisms at the human FMO3 gene locus.

Hao DC, Sun J, Furnes B, Schlenk D, Hou ZF, Zhang YP, Yang SL, Yang L.

Biochem Genet. 2006 Oct;44(7-8):391-407. Epub 2006 Nov 10.

PMID:
17096187
14.

Haplotype tagging for the identification of common disease genes.

Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, Cordell HJ, Eaves IA, Dudbridge F, Twells RC, Payne F, Hughes W, Nutland S, Stevens H, Carr P, Tuomilehto-Wolf E, Tuomilehto J, Gough SC, Clayton DG, Todd JA.

Nat Genet. 2001 Oct;29(2):233-7.

PMID:
11586306
15.

Strong linkage disequilibrium at the nucleotide analogue transporter ABCC5 gene locus.

Gwee PC, Tang K, Sew PH, Lee EJ, Chong SS, Lee CG.

Pharmacogenet Genomics. 2005 Feb;15(2):91-104.

PMID:
15861033
16.

[Haplotypes of four single nucleotide polymorphisms in caspase-8, -10 genes in Han nationality of Zhejiang province in China].

Ye YF, Zhou R, Xie Y, Yang SY, Zhang W.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Apr;23(2):222-6. Chinese.

PMID:
16604504
17.

Prion gene haplotypes of U.S. cattle.

Clawson ML, Heaton MP, Keele JW, Smith TP, Harhay GP, Laegreid WW.

BMC Genet. 2006 Nov 8;7:51.

18.

Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype.

Kim KS, Kim GS, Hwang JY, Lee HJ, Park MH, Kim KJ, Jung J, Cha HS, Shin HD, Kang JH, Park EK, Kim TH, Hong JM, Koh JM, Oh B, Kimm K, Kim SY, Lee JY.

BMC Med Genet. 2007 Nov 26;8:70.

20.

Evaluation of linkage disequilibrium between chromosome 22q11 single nucleotide polymorphisms in a large outbred population.

Shaw SH, Hutchison D, Saiz R, Abel K, DeLisi LE, Schork NJ, Sherrington R.

Am J Med Genet. 2002 Mar 8;114(2):205-13.

PMID:
11857583

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