Germline hypermethylation of the APC promotor is not a frequent cause of familial adenomatous polyposis in APC/MUTYH mutation negative families
Published: International Journal of Cancer, 2008, 122:1422-5
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Archived publications
older then 10 yearsGastrointestinal polyposis syndromes
Published: In: Allgayer H, Rehder H, Fulda S (eds): Hereditary tumors. Wiley-VCH Verlag, 2008, S. 257-280.
First Description of a Case of Classic Maternal Phenylketonuria and Sonographic Signs of Fetal Trisomy 21
Published: XXIV International Congress "The Fetus as a Patient", Frankfurt 2008; S. 93-97
Absent immunoglobulins in HIV-related Burkitt lymphoma/leukaemia
Published: Annals Hemantology (2008) 87.3; S. 255-256
MLD according to the WHO classification in AML has no correlation with age and no independent prognostic relevance as analyzed in 1766 patients
Published: Blood (2008), 111(4), S. 1855-1861
High proportion of large genomic deletions and a genotype-phenotype update in 80 unrelated families with juvenile polyposis syndrome
Published: Journal of Medical Genetics, 2007, 44:702-709
Corticobasal degeneration presenting with progressive spasticity
Published: NEUROLOGY 68 (2007); S. 791-792
A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation
Published: NEUROLOGY 69 (2007); S. 368-375
Establishment and characterization of two uveal melanoma cell lines derived from tumors with loss of one chromosome
Published: 3. Exp Eye Res. 2006 Oct; 83(4);Epub 2006 Jun 5. Review. PMID: 16750193; S. 858-64;
Predictive testing and genetic counselling
Published: Encyclopedic Reference of Genomics and Proteomics in Molecular Medicine, D Ganten, K Ruckpaul (ea); 2006, S. 1453-1456
Archived publications
before 2003- Publications before 2003
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