W Friedl|T Fritz - JoVE Visualize

Showing results (101-110 of 256) with videos related to

Pageof 26

Sort By:

American Journal of Medical Genetics|December 23, 1999

ADULT syndrome allelic to limb mammary syndrome (LMS)?P Propping, W Friedl, T F Wienker, et al.

Atherosclerosis|October 1, 1988

Genetic variation in the apolipoprotein AI-CIII-AIV gene cluster and coronary heart diseaseB Paulweber, W Friedl, F Krempler, et al.

Human Genetics|January 1, 1981

Quantitative and qualitative assay of amniotic-fluid acetylcholinesterase in the prenatal diagnosis of neural tube defectsT Voigtländer, W Friedl, M Cremer, et al.

The American Journal of Gastroenterology|November 6, 2001

A de novo deletion of chromosome 5q causing familial adenomatous polyposis, dysmorphic features, and mild mental retardationJ Raedle, W Friedl, H Engels, et al.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 6, 1998

[Val384Asp in hMLH1 gene in Chinese, Japanese and German and its etiological role in colorectal cancer]Y Wang, W Friedl, P Propping, et al.

Human Molecular Genetics|January 1, 1994

Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposisM Mandl, R Paffenholz, W Friedl, et al.

Human Genetics|April 1, 1989

Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implicationsC Hohenschutz, P Eich, W Friedl, et al.

Human Genetics|September 1, 1997

Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissueY Wang, W Friedl, C Lamberti, et al.

Developmental Neuroscience|January 1, 1991

Phenotypic consequences of low arylsulfatase A genotypes (ASAp/ASAp and ASA-/ASAp): does there exist an association with multiple sclerosis?J Kappler, W Pötter, V Gieselmann, et al.

American Journal of Medical Genetics|October 1, 1991

MASA syndrome: clinical variability and linkage analysisM Rietschel, W Friedl, S Uhlhaas, et al.

Pageof 26

Showing results (101-110 of 256) with videos related to

Sort By:

Pageof 26

American Journal of Medical Genetics|December 23, 1999

ADULT syndrome allelic to limb mammary syndrome (LMS)?P Propping, W Friedl, T F Wienker, et al.

Atherosclerosis|October 1, 1988

Genetic variation in the apolipoprotein AI-CIII-AIV gene cluster and coronary heart diseaseB Paulweber, W Friedl, F Krempler, et al.

Human Genetics|January 1, 1981

Quantitative and qualitative assay of amniotic-fluid acetylcholinesterase in the prenatal diagnosis of neural tube defectsT Voigtländer, W Friedl, M Cremer, et al.

The American Journal of Gastroenterology|November 6, 2001

A de novo deletion of chromosome 5q causing familial adenomatous polyposis, dysmorphic features, and mild mental retardationJ Raedle, W Friedl, H Engels, et al.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 6, 1998

[Val384Asp in hMLH1 gene in Chinese, Japanese and German and its etiological role in colorectal cancer]Y Wang, W Friedl, P Propping, et al.

Human Molecular Genetics|January 1, 1994

Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposisM Mandl, R Paffenholz, W Friedl, et al.

Human Genetics|April 1, 1989

Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implicationsC Hohenschutz, P Eich, W Friedl, et al.

Human Genetics|September 1, 1997

Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissueY Wang, W Friedl, C Lamberti, et al.

Developmental Neuroscience|January 1, 1991

Phenotypic consequences of low arylsulfatase A genotypes (ASAp/ASAp and ASA-/ASAp): does there exist an association with multiple sclerosis?J Kappler, W Pötter, V Gieselmann, et al.

American Journal of Medical Genetics|October 1, 1991

MASA syndrome: clinical variability and linkage analysisM Rietschel, W Friedl, S Uhlhaas, et al.

Pageof 26