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457 Assessment of BRAF, NRAS, KRAS and EGFR mutation status in thyroid nodules

European journal of cancer (1990), 2015-09, Vol.51, p.S97-S97

2015

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580: Sensitive detection of NRAS mutations using mutant-enriched PCR and reverse-hybridization teststrips

European journal of cancer (1990), 2014-07, Vol.50, p.S139-S140

2014

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Stable preservation of SARS-COV-2 RNA from gargle samples on FTA cards

Clinica chimica acta, 2024-05, Vol.558, p.119143, Article 119143

2024

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BRAF mutational epidemiology in dysplastic nevi: Does different solar UV radiation exposure matter?

Journal of the European Academy of Dermatology and Venereology, 2014-05, Vol.28 (5), p.615-625

2014

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W101 Stable preservation of SARS-COV-2 RNA from gargle samples on FTA cards

Clinica chimica acta, 2022-05, Vol.530, p.S320-S320

2022

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BRAF mutation status in primary and metastatic melanomas in two regions with differing potential ultraviolet radiation exposure

Clinical and experimental dermatology, 2014-12, Vol.39 (8), p.932-943

2014

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6 A novel StripAssay for the detection of cystic fibrosis mutations in the Turkish population

Journal of cystic fibrosis, 2012-06, Vol.11, p.S56-S56

2012

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Association between serum amyloid A1 genotype and age of onset restricts to M694 homozygote familial Mediterranean fever patients in Armenia

Clinical and Experimental Rheumatology, 2021-09, Vol.39 Suppl 132 (5), p.18-21

2021

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Simultaneous detection of common cystic fibrosis mutations by reverse-hybridization teststrips

Journal of cystic fibrosis, 2010, Vol.9, p.S13-S13

2010

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24 Multicenter validation study of a novel StripAssay for cystic fibrosis

Journal of cystic fibrosis, 2011, Vol.10, p.S7-S7

2011

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ALPHA- AND BETA-GLOBIN GENE MUTATIONS IN GEORGIA AND ARMENIA

Georgian medical news, 2021-09 (318), p.124-128

2021

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189 Sensitive detection of KRAS and BRAF mutations using mutant-enriched PCR and reverse-hybridization teststrips

European journal of cancer supplements, 2010, Vol.8 (5), p.49-50

2010

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1145 - Sensitive Detection of BRAF Mutations Using Mutant-Enriched PCR and Reverse-Hybridization Teststrips

Annals of oncology, 2012-09, Vol.23, p.ix373-ix373

2012

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Sensitive Detection of BRAF Mutations Using Mutant-Enriched PCR and Reverse-Hybridization Teststrips

Annals of oncology, 2012-09, Vol.23, p.ix373

2012

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Molecular diagnosis of hereditary hemochromatosis: application of a newly-developed reverse-hybridization assay in the South African population

Clinical genetics, 2004-04, Vol.65 (4), p.317-321

2004

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Prevalence of HFE mutations in upper Northern Italy: study of 1132 unrelated blood donors

Digestive and liver disease, 2003-07, Vol.35 (7), p.479-481

2003

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Plasminogen activator inhibitor I 4G/5G polymorphism and coagulation Factor XIII Val34Leu polymorphism: Impaired fibrinolysis and early pregnancy loss

Clinical chemistry (Baltimore, Md.), 2003-07, Vol.49 (7), p.1081-1086

2003

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P02-019 - Detection of risk factors for AA-amyloidosis

Pediatric rheumatology online journal, 2013-11, Vol.11 (S1), p.A126-A126, Article A126

2013

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Molecular mechanisms underlying thalassemia intermedia in Iran

Genetic testing, 2008-12, Vol.12 (4), p.549-556

2008

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Investigation of Genetic Variants of Genes of the Hemochromatosis Pathway and Their Role in Breast Cancer

Cancer epidemiology, biomarkers & prevention, 2005-05, Vol.14 (5), p.1102-1107

2005

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Elevated coagulation factor VIII and the risk for recurrent early pregnancy loss

Thrombosis and haemostasis, 2004-04, Vol.91 (4), p.694-699

2004

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alpha-globin gene deletion and point mutation analysis among in Iranian patients with microcytic hypochromic anemia

Haematologica (Roma), 2003-10, Vol.88 (10), p.1196

2003

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Phenotypic expression of the C282Y/Q283P compound heterozygosity in HFE and molecular modeling of the Q283P mutation effect

Blood cells, molecules, & diseases, 2003-09, Vol.31 (2), p.173-173

Oberkanins, Dr.Christian

2003

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Rare and unexpected mutations among Iranian beta-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing

Haematologica (Roma), 2002-10, Vol.87 (10), p.1113

2002

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Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestry

Haematologica (Roma), 2003-03, Vol.88 (3), p.250

2003

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457 Assessment of BRAF, NRAS, KRAS and EGFR mutation status in thyroid nodules

580: Sensitive detection of NRAS mutations using mutant-enriched PCR and reverse-hybridization teststrips

Stable preservation of SARS-COV-2 RNA from gargle samples on FTA cards

BRAF mutational epidemiology in dysplastic nevi: Does different solar UV radiation exposure matter?

W101 Stable preservation of SARS-COV-2 RNA from gargle samples on FTA cards

BRAF mutation status in primary and metastatic melanomas in two regions with differing potential ultraviolet radiation exposure

6 A novel StripAssay for the detection of cystic fibrosis mutations in the Turkish population

Association between serum amyloid A1 genotype and age of onset restricts to M694 homozygote familial Mediterranean fever patients in Armenia

Simultaneous detection of common cystic fibrosis mutations by reverse-hybridization teststrips

24 Multicenter validation study of a novel StripAssay for cystic fibrosis

ALPHA- AND BETA-GLOBIN GENE MUTATIONS IN GEORGIA AND ARMENIA

189 Sensitive detection of KRAS and BRAF mutations using mutant-enriched PCR and reverse-hybridization teststrips

1145 - Sensitive Detection of BRAF Mutations Using Mutant-Enriched PCR and Reverse-Hybridization Teststrips

Sensitive Detection of BRAF Mutations Using Mutant-Enriched PCR and Reverse-Hybridization Teststrips

Molecular diagnosis of hereditary hemochromatosis: application of a newly-developed reverse-hybridization assay in the South African population

Prevalence of HFE mutations in upper Northern Italy: study of 1132 unrelated blood donors

Plasminogen activator inhibitor I 4G/5G polymorphism and coagulation Factor XIII Val34Leu polymorphism: Impaired fibrinolysis and early pregnancy loss

P02-019 - Detection of risk factors for AA-amyloidosis

Molecular mechanisms underlying thalassemia intermedia in Iran

Investigation of Genetic Variants of Genes of the Hemochromatosis Pathway and Their Role in Breast Cancer

Elevated coagulation factor VIII and the risk for recurrent early pregnancy loss

alpha-globin gene deletion and point mutation analysis among in Iranian patients with microcytic hypochromic anemia

Phenotypic expression of the C282Y/Q283P compound heterozygosity in HFE and molecular modeling of the Q283P mutation effect

Rare and unexpected mutations among Iranian beta-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing

Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestry

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