Archiv

Dezember 2007

Autor(en): Romero-Giménez J, Dopeso H, Blanco I, Guerra-Moreno A, Gonzalez S, Vogt S, Aretz S, Schwartz S Jr, Capella G, Arango D

Germline hypermethylation of the APC promotor is not a frequent cause of familial adenomatous polyposis in APC/MUTYH mutation negative families

Publiziert: International Journal of Cancer, 2008, 122:1422-5

Dezember 2007

Autor(en): Friedl W, Vogt S

Gastrointestinal polyposis syndromes

Publiziert: In: Allgayer H, Rehder H, Fulda S (eds): Hereditary tumors. Wiley-VCH Verlag, 2008, S. 257-280.

Dezember 2007

Autor(en): Lehnen H., Vinke M., Schwennicke G, Pascheberg U

First Description of a Case of Classic Maternal Phenylketonuria and Sonographic Signs of Fetal Trisomy 21

Publiziert: XXIV International Congress "The Fetus as a Patient", Frankfurt 2008; S. 93-97

Dezember 2007

Autor(en): Shimomura A, Lilienfeld-Toal M, Balta Z,Schroers E, Schmidt-Wolf I, Büttner R, Rücker A, Gütgemann I

Absent immunoglobulins in HIV-related Burkitt lymphoma/leukaemia

Publiziert: Annals Hemantology (2008) 87.3; S. 255-256

Dezember 2007

Autor(en): Wandt H, Schäkel U, Kroschinsky F, Prange-Krex G, Mohr B, Thiede C, Pascheberg U, Soucek S, Schaich M, Ehninger G.

MLD according to the WHO classification in AML has no correlation with age and no independent prognostic relevance as analyzed in 1766 patients

Publiziert: Blood (2008), 111(4), S. 1855-1861

Dezember 2006

Autor(en): Aretz S, Stienen D, Uhlhaas S, Stolte M, Entius MM, Loff S, Back W, Kaufmann A, Keller K-M, Blaas SH, Siebert R, Vogt S, Spranger S, Holinski-Feder E, Sunde L, Propping P, Friedl W

High proportion of large genomic deletions and a genotype-phenotype update in 80 unrelated families with juvenile polyposis syndrome

Publiziert: Journal of Medical Genetics, 2007, 44:702-709

Dezember 2006

Autor(en): Hasselblatt M, S Föllinger, P Steinbach, A Schwan, W Paulus

Corticobasal degeneration presenting with progressive spasticity

Publiziert: NEUROLOGY 68 (2007); S. 791-792

Dezember 2006

Autor(en): Warnecke T, Duning T, Schwan A, Lohmann H, Epplen JT, Young P

A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation

Publiziert: NEUROLOGY 69 (2007); S. 368-375

Oktober 2006

Autor(en): Nareyeck G., Zeschnigk M., Prescher G., Lohmann D.R., Anastassiou G.

Establishment and characterization of two uveal melanoma cell lines derived from tumors with loss of one chromosome

Publiziert: 3. Exp Eye Res. 2006 Oct; 83(4);Epub 2006 Jun 5. Review. PMID: 16750193; S. 858-64;

Dezember 2005

Autor(en): Schwan A, JT Epplen

Predictive testing and genetic counselling

Publiziert: Encyclopedic Reference of Genomics and Proteomics in Molecular Medicine, D Ganten, K Ruckpaul (ea); 2006, S. 1453-1456

Archiv

Archivierte Veröffentlichungen

Germline hypermethylation of the APC promotor is not a frequent cause of familial adenomatous polyposis in APC/MUTYH mutation negative families

Gastrointestinal polyposis syndromes

First Description of a Case of Classic Maternal Phenylketonuria and Sonographic Signs of Fetal Trisomy 21

Absent immunoglobulins in HIV-related Burkitt lymphoma/leukaemia

MLD according to the WHO classification in AML has no correlation with age and no independent prognostic relevance as analyzed in 1766 patients

High proportion of large genomic deletions and a genotype-phenotype update in 80 unrelated families with juvenile polyposis syndrome

Corticobasal degeneration presenting with progressive spasticity

A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation

Establishment and characterization of two uveal melanoma cell lines derived from tumors with loss of one chromosome

Predictive testing and genetic counselling

Archivierte Veröffentlichungen

Aktuelle Veröffentlichungen

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Laboratoriumsmedizin

Laboratoriumsmedizin

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Mikrobiologie, Infektions-PCR

Mikrobiologie

Infektions-PCR

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Analytik Laboratoriumsmedizin und Humangenetik

Haus 4 - Hansakontor

Endokrinologie, Diabetologie, Rheumatologie, Humangenetik, Schulungszentrum

Zentrum für Endokrinologie, Diabetologie, Rheumatologie

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Hormon- und Stoffwechselzentrum für Kinder und Jugendliche

Hormonzentrum für Kinder und Jugendliche