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W Friedl

Showing results (141-150 of 194) with videos related to

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Cancer Detection and Prevention|March 29, 2001
Detection of APC and k-ras mutations in the serum of patients with colorectal cancerH Lauschke, R Caspari, W Friedl, et al.
Human Genetics|May 1, 1996
Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC proteinW Friedl, S Meuschel, R Caspari, et al.
Archives of Orthopaedic and Trauma Surgery|January 1, 1992
Diagnosis and treatment of retroperitoneal hematoma in multiple trauma patientsT Hölting, H J Buhr, G M Richter, et al.
Deutsche Medizinische Wochenschrift (1946)|March 4, 2000
[The diagnosis of hereditary colorectal carcinomas]R Caspari, M Jungck, C Lamberti, et al.
The Journal of Investigative Dermatology|January 14, 1999
A novel germline mutation in the hMLH1 DNA mismatch repair gene in a patient with an isolated cystic sebaceous tumorR Kruse, A Rütten, H R Malayeri, et al.
The British Journal of Dermatology|June 1, 1997
Muir-Torre syndrome: clinical features and molecular genetic analysisC Esche, R Kruse, C Lamberti, et al.
Human Mutation|January 1, 1997
Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genesM Wehner, L Buschhausen, C Lamberti, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|October 1, 1987
[Significance of primary radical surgery for survival following treatment of breast cancer. Problems of interpretation of treatment results of prospective, nonrandomized studies exemplified by the Southwest Germany Breast Cancer Study]W Friedl, B Henningsen, U Abel, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 14, 2005
Analysis of germline mutations in the APC gene in familial adenomatous polyposis patientsXiao-rong Liu, Xiang-nian Shan, W Friedl, et al.
American Journal of Medical Genetics|September 1, 1988
Probable metachromatic leukodystrophy/pseudodeficiency compound heterozygote at the arylsulfatase A locus with neurological and psychiatric symptomatologyC Hohenschutz, W Friedl, K H Schlör, et al.
Pageof 20

Showing results (141-150 of 194) with videos related to

Sort By:
Pageof 20
Cancer Detection and Prevention|March 29, 2001
Detection of APC and k-ras mutations in the serum of patients with colorectal cancerH Lauschke, R Caspari, W Friedl, et al.
Human Genetics|May 1, 1996
Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC proteinW Friedl, S Meuschel, R Caspari, et al.
Archives of Orthopaedic and Trauma Surgery|January 1, 1992
Diagnosis and treatment of retroperitoneal hematoma in multiple trauma patientsT Hölting, H J Buhr, G M Richter, et al.
Deutsche Medizinische Wochenschrift (1946)|March 4, 2000
[The diagnosis of hereditary colorectal carcinomas]R Caspari, M Jungck, C Lamberti, et al.
The Journal of Investigative Dermatology|January 14, 1999
A novel germline mutation in the hMLH1 DNA mismatch repair gene in a patient with an isolated cystic sebaceous tumorR Kruse, A Rütten, H R Malayeri, et al.
The British Journal of Dermatology|June 1, 1997
Muir-Torre syndrome: clinical features and molecular genetic analysisC Esche, R Kruse, C Lamberti, et al.
Human Mutation|January 1, 1997
Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genesM Wehner, L Buschhausen, C Lamberti, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|October 1, 1987
[Significance of primary radical surgery for survival following treatment of breast cancer. Problems of interpretation of treatment results of prospective, nonrandomized studies exemplified by the Southwest Germany Breast Cancer Study]W Friedl, B Henningsen, U Abel, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 14, 2005
Analysis of germline mutations in the APC gene in familial adenomatous polyposis patientsXiao-rong Liu, Xiang-nian Shan, W Friedl, et al.
American Journal of Medical Genetics|September 1, 1988
Probable metachromatic leukodystrophy/pseudodeficiency compound heterozygote at the arylsulfatase A locus with neurological and psychiatric symptomatologyC Hohenschutz, W Friedl, K H Schlör, et al.
Pageof 20