H K Schackert|C Kruppa|M Hahn - JoVE Visualize

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Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|February 5, 1999

[The Human Genome Project and its consequences for surgery]H K Schackert, C Kruppa, M Hahn

Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|February 5, 1999

[Basic molecular biology of colon and rectal carcinoma--when differential diagnosis?]H K Schackert, C Kruppa, M Hahn

Zentralblatt Fur Chirurgie|June 4, 1999

[Predictive molecular diagnosis and preventive surgical treatment of hereditary colorectal carcinoma: a new field of interest for surgical research]M Hahn, C Kruppa, S Pistorius, et al.

International Journal of Colorectal Disease|January 27, 2000

Hereditary colorectal cancer: clinical consequences of predictive molecular testingM Hahn, H D Saeger, H K Schackert

Langenbeck'S Archives of Surgery|January 28, 1999

Molecular biology of colorectal cancer and clinical consequences for colorectal cancer syndromesM Hahn, O N Koufaki, H K Schackert

Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|June 4, 1999

[Preventive surgery of inherited colorectal cancer identified through molecular diagnosis]H K Schackert, M Hahn, S Pistorius, et al.

Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|October 2, 2003

[Molecular diagnosis and clinical consequences in families with HNPCC syndrome]S Pistorius, J Plaschke, C Kruppa, et al.

Biotechniques|May 20, 1998

Doublex sequencing in molecular diagnosis of hereditary diseasesJ Plaschke, H Voss, M Hahn, et al.

International Journal of Colorectal Disease|January 5, 2002

Combined molecular and clinical approach for decision making for surgery in HNPCC patients: a report on three cases in two familiesS R Pistorius, M Nagel, S Kruger, et al.

Journal of Neuro-Oncology|February 24, 2001

Frequent loss of heterozygosity at the 19p13.3 locus without LKB1/STK11 mutations in human carcinoma metastases to the brainS B Sobottka, M Haase, G Fitze, et al.

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Showing results (1-10 of 1,264) with videos related to

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Pageof 127

Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|February 5, 1999

[The Human Genome Project and its consequences for surgery]H K Schackert, C Kruppa, M Hahn

Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|February 5, 1999

[Basic molecular biology of colon and rectal carcinoma--when differential diagnosis?]H K Schackert, C Kruppa, M Hahn

Zentralblatt Fur Chirurgie|June 4, 1999

[Predictive molecular diagnosis and preventive surgical treatment of hereditary colorectal carcinoma: a new field of interest for surgical research]M Hahn, C Kruppa, S Pistorius, et al.

International Journal of Colorectal Disease|January 27, 2000

Hereditary colorectal cancer: clinical consequences of predictive molecular testingM Hahn, H D Saeger, H K Schackert

Langenbeck'S Archives of Surgery|January 28, 1999

Molecular biology of colorectal cancer and clinical consequences for colorectal cancer syndromesM Hahn, O N Koufaki, H K Schackert

Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|June 4, 1999

[Preventive surgery of inherited colorectal cancer identified through molecular diagnosis]H K Schackert, M Hahn, S Pistorius, et al.

Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|October 2, 2003

[Molecular diagnosis and clinical consequences in families with HNPCC syndrome]S Pistorius, J Plaschke, C Kruppa, et al.

Biotechniques|May 20, 1998

Doublex sequencing in molecular diagnosis of hereditary diseasesJ Plaschke, H Voss, M Hahn, et al.

International Journal of Colorectal Disease|January 5, 2002

Combined molecular and clinical approach for decision making for surgery in HNPCC patients: a report on three cases in two familiesS R Pistorius, M Nagel, S Kruger, et al.

Journal of Neuro-Oncology|February 24, 2001

Frequent loss of heterozygosity at the 19p13.3 locus without LKB1/STK11 mutations in human carcinoma metastases to the brainS B Sobottka, M Haase, G Fitze, et al.

Pageof 127