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Assessment of three mitochondrial genes (16S, Cytb, CO1) for identifying species in the Praomyini tribe (Rodentia: Muridae)

PloS one, 2012-05, Vol.7 (5), p.e36586-e36586

2012

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Full-length transcript amplification and sequencing as universal method to test mRNA integrity and biallelic expression in mismatch repair genes

European journal of human genetics : EJHG, 2019-12, Vol.27 (12), p.1808-1820

2019

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Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome

Journal of medical genetics, 2011-08, Vol.48 (8), p.513-519

2011

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Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families

International journal of cancer, 2014-07, Vol.135 (1), p.69-77

2014

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Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3

Carcinogenesis (New York), 2014-02, Vol.35 (2), p.315-323

2014

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Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012

European journal of human genetics : EJHG, 2013-01, Vol.21 (1), p.118-118

2013

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Clinical utility gene card for: Lynch syndrome ( , , , )

European journal of human genetics : EJHG, 2010-09, Vol.18 (9), p.1071-1071

2010

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Adjuvant chemotherapy (ACT) in stage II colon cancer (CC) in patients with Lynch syndrome

Journal of clinical oncology, 2012-05, Vol.30 (15_suppl), p.3550-3550

2012

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Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies

Familial cancer, 2011-06, Vol.10 (2), p.273-284

2011

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No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients

European journal of human genetics : EJHG, 2008-05, Vol.16 (5), p.587-592

2008

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No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients. Commentary

European journal of human genetics : EJHG, 2008, Vol.16 (5)

2008

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Notiz zur photometrischen Bestimmung von Triphenylmethanol ber das Triphenylmethylkation

Fresenius Zeitschrift für Analytische Chemie, 1972, Vol.259 (2), p.115-118

1972

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Assessment of three mitochondrial genes (16S, Cytb, CO1) for identifying species in the Praomyini tribe (Rodentia: Muridae)

Full-length transcript amplification and sequencing as universal method to test mRNA integrity and biallelic expression in mismatch repair genes

Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome

Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families

Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3

Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012

Clinical utility gene card for: Lynch syndrome ( , , , )

Adjuvant chemotherapy (ACT) in stage II colon cancer (CC) in patients with Lynch syndrome

Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies

No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients

No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients. Commentary

Notiz zur photometrischen Bestimmung von Triphenylmethanol ber das Triphenylmethylkation

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