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Items: 1 to 20 of 94

1.

Rapid multiplexed genotyping for hereditary thrombophilia by SELDI-TOF mass spectrometry.

Yang S, Xu L, Wu HM.

Diagn Mol Pathol. 2010 Mar;19(1):54-61. doi: 10.1097/PDM.0b013e3181a814bf.

PMID:
20186013
5.

Detection of genomic polymorphisms associated with venous thrombosis using the invader biplex assay.

Patnaik M, Dlott JS, Fontaine RN, Subbiah MT, Hessner MJ, Joyner KA, Ledford MR, Lau EC, Moehlenkamp C, Amos J, Zhang B, Williams TM.

J Mol Diagn. 2004 May;6(2):137-44.

6.

Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.

Rahimi Z, Nomani H, Mozafari H, Vaisi-Raygani A, Madani H, Malek-Khosravi S, Parsian A.

Blood Coagul Fibrinolysis. 2009 Jun;20(4):252-6. doi: 10.1097/MBC.0b013e3283255487.

PMID:
19349859
7.

An Arab selective gradient in the distribution of factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase (MTHFR) C677T.

Ameen G, Irani-Hakime N, Fawaz NA, Mahjoub T, Almawi WY.

J Thromb Haemost. 2005 Sep;3(9):2126-7. No abstract available.

8.

Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for genotyping of human platelet-specific antigens.

Garritsen HS, Fan AX, Bosse N, Hannig H, Kelsch R, Kroll H, Holzgreve W, Zhong XY.

Transfusion. 2009 Feb;49(2):252-8. doi: 10.1111/j.1537-2995.2008.01953.x. Epub 2008 Oct 29.

PMID:
18980617
9.
10.

Primer-engineered multiplex PCR-RFLP for detection of MTHFR C677T, prothrombin G20210A and factor V Leiden mutations.

Koksal V, Baris I, Etlik O.

Exp Mol Pathol. 2007 Aug;83(1):1-3. Epub 2006 Dec 30.

PMID:
17275807
11.

Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR G677A among 594 thrombotic Jordanian patients.

Eid SS, Shubeilat T.

Blood Coagul Fibrinolysis. 2005 Sep;16(6):417-21.

PMID:
16093732
12.

High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise.

Bray MS, Boerwinkle E, Doris PA.

Hum Mutat. 2001 Apr;17(4):296-304.

PMID:
11295828
13.

Analytical validation of the tag-it high-throughput microsphere-based universal array genotyping platform: application to the multiplex detection of a panel of thrombophilia-associated single-nucleotide polymorphisms.

Bortolin S, Black M, Modi H, Boszko I, Kobler D, Fieldhouse D, Lopes E, Lacroix JM, Grimwood R, Wells P, Janeczko R, Zastawny R.

Clin Chem. 2004 Nov;50(11):2028-36. Epub 2004 Sep 13.

14.

[Genetic determinants of hereditary thrombophilia in pathogenesis of venous thrombosis].

Kapustin SI, Blinov MN, Kargin VD, Filanovskaia LI, Saltykova NB, Beliazo OE, Golovina OG, Shmeleva VM, Panshina AM, Papaian LP.

Ter Arkh. 2003;75(10):78-80. Russian.

PMID:
14669613
15.

Genetic testing for thrombophilia mutations.

Hertzberg MS.

Semin Thromb Hemost. 2005 Feb;31(1):33-8. Review.

PMID:
15706473
16.

Genotyping of single-nucleotide polymorphisms by high-resolution melting of small amplicons.

Liew M, Pryor R, Palais R, Meadows C, Erali M, Lyon E, Wittwer C.

Clin Chem. 2004 Jul;50(7):1156-64.

18.

Legg-perthes disease and heritable thrombophilia.

López-Franco M, González-Morán G, De Lucas JC Jr, Llamas P, de Velasco JF, Vivancos JC, Epeldegui-Torre T.

J Pediatr Orthop. 2005 Jul-Aug;25(4):456-9.

PMID:
15958894
19.

A new PCR-SSP typing method for six single-nucleotide polymorphisms impairing the blood-clotting cascade as well as T-cell stimulation.

Meyer M, Czachurski D, Tran TH, Opelz G, Mytilineos J.

Tissue Antigens. 2005 Dec;66(6):650-5. Erratum in: Tissue Antigens. 2006 Mar;67(3):265. Hien, T [corrected to Tran, TH].

PMID:
16305681
20.

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