249 related articles for article (PubMed ID: 11857746)
21. Comprehensive and efficient HBB mutation analysis for detection of beta-hemoglobinopathies in a pan-ethnic population.
Chan OT; Westover KD; Dietz L; Zehnder JL; Schrijver I
Am J Clin Pathol; 2010 May; 133(5):700-7. PubMed ID: 20395516
[TBL] [Abstract][Full Text] [Related]
22. Rapid and accurate detection of atypical and Kalow variants in the butyrylcholinesterase gene using denaturing high performance liquid chromatography.
Levano S; Keller D; Schobinger E; Urwyler A; Girard T
Anesth Analg; 2008 Jan; 106(1):147-51, table of contents. PubMed ID: 18165570
[TBL] [Abstract][Full Text] [Related]
23. A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosis.
Fucharoen S; Fucharoen G; Ratanasiri T; Jetsrisuparb A; Fukumaki Y
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():278-81. PubMed ID: 8629124
[TBL] [Abstract][Full Text] [Related]
24. DHPLC screening of cystic fibrosis gene mutations.
Ravnik-Glavac M; Atkinson A; Glavac D; Dean M
Hum Mutat; 2002 Apr; 19(4):374-83. PubMed ID: 11933191
[TBL] [Abstract][Full Text] [Related]
25. Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC).
Sahli CA; Ben Salem I; Jouini L; Laouini N; Dabboubi R; Hadj Fredj S; Siala H; Othmeni R; Dakhlaoui B; Fattoum S; Bibi A; Messaoud T
J Clin Lab Anal; 2016 Sep; 30(5):392-8. PubMed ID: 27086580
[TBL] [Abstract][Full Text] [Related]
26. Development of a denaturing high-performance liquid chromatography screening method for SMAD4 in juvenile polyposis syndrome.
Hatch SL; Trewick AL; Payne SJ
Ann Clin Biochem; 2007 Mar; 44(Pt 2):159-63. PubMed ID: 17362581
[TBL] [Abstract][Full Text] [Related]
27. Validation of dHPLC for molecular diagnosis of beta-thalassemia in Southern Italy.
Colosimo A; Guida V; Scolari A; De Luca A; Palka G; Rigoli L; Meo A; Salpietro DC; Dallapiccola B
Genet Test; 2003; 7(3):269-75. PubMed ID: 14642006
[TBL] [Abstract][Full Text] [Related]
28. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
Basak AN
Hemoglobin; 2007; 31(2):233-41. PubMed ID: 17486506
[TBL] [Abstract][Full Text] [Related]
29. Denaturing high-performance liquid chromatography (DHPLC)-based prenatal diagnosis for tuberous sclerosis.
Bénit P; Bonnefont JP; Kara Mostefa A; Francannet C; Munnich A; Ray PF
Prenat Diagn; 2001 Apr; 21(4):279-83. PubMed ID: 11288117
[TBL] [Abstract][Full Text] [Related]
30. Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone disease.
Yu B; Sawyer NA; Caramins M; Yuan ZG; Saunderson RB; Pamphlett R; Richmond DR; Jeremy RW; Trent RJ
J Clin Pathol; 2005 May; 58(5):479-85. PubMed ID: 15858117
[TBL] [Abstract][Full Text] [Related]
31. Enhanced detection of TP53 mutations using a GC-clamp in denaturing high performance liquid chromatography.
Greiner TC
Diagn Mol Pathol; 2007 Mar; 16(1):32-7. PubMed ID: 17471156
[TBL] [Abstract][Full Text] [Related]
32. Genotyping of β-globin gene mutations in single lymphocytes: a preliminary study for preimplantation genetic diagnosis of monogenic disorders.
Durmaz B; Ozkinay F; Onay H; Karaca E; Aydinok Y; Tavmergen E; Vrettou C; Traeger-Synodinos J; Kanavakis E
Hemoglobin; 2012; 36(3):230-43. PubMed ID: 22524255
[TBL] [Abstract][Full Text] [Related]
33. Molecular heterogeneity of beta-thalassemia alleles in Spain and its importance in the diagnosis and prevention of beta-thalassemia major and sickle cell disorders.
Pereira Mdel M; Dalmau AC; Corrons JL
Hemoglobin; 2009; 33(3):226-34. PubMed ID: 19657837
[TBL] [Abstract][Full Text] [Related]
34. Real-time PCR for single-cell genotyping in sickle cell and thalassemia syndromes as a rapid, accurate, reliable, and widely applicable protocol for preimplantation genetic diagnosis.
Vrettou C; Traeger-Synodinos J; Tzetis M; Palmer G; Sofocleous C; Kanavakis E
Hum Mutat; 2004 May; 23(5):513-21. PubMed ID: 15108284
[TBL] [Abstract][Full Text] [Related]
35. NF1 gene analysis based on DHPLC.
De Luca A; Buccino A; Gianni D; Mangino M; Giustini S; Richetta A; Divona L; Calvieri S; Mingarelli R; Dallapiccola B
Hum Mutat; 2003 Feb; 21(2):171-2. PubMed ID: 12552569
[TBL] [Abstract][Full Text] [Related]
36. Prenatal diagnosis of beta-thalassaemia mutations using the reverse dot blot technique.
Muralitharan S; Srivastava A; Shaji RV; Mathai M; Srivastava VM; Dennison D; Lu CY; Krishnamoorthy R
Natl Med J India; 1996; 9(2):70-1. PubMed ID: 8857041
[TBL] [Abstract][Full Text] [Related]
37. Denaturing high-performance liquid chromatography technique platform applied to screen G6PD deficient variants.
Jiang WY; Chen LM; Lin QD; Geng Q; Du CS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):607-11. PubMed ID: 16331553
[TBL] [Abstract][Full Text] [Related]
38. Spatially addressable bead-based biosensor for rapid detection of beta-thalassemia mutations.
Ng JK; Wang W; Liu WT; Chong SS
Anal Chim Acta; 2010 Jan; 658(2):193-6. PubMed ID: 20103094
[TBL] [Abstract][Full Text] [Related]
39. Screening of beta-thalassemia mutations by PCR and ASO analysis in an Italian population of mixed geographic origin.
Alfarano A; Gottardi E; Serra A; Piga A; Mandrino M; Mazza U; Camaschella C
Haematologica; 1990; 75(6):506-9. PubMed ID: 2098291
[TBL] [Abstract][Full Text] [Related]
40. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
Jensen HK
Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]