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W Friedl

Showing results (151-160 of 194) with videos related to

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Zeitschrift Fur Gastroenterologie|November 1, 1993
Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methodsR Caspari, W Friedl, T Böker, et al.
Human Genetics|February 1, 1996
Familial adenomatous polyposis: a submicroscopic deletion at the APC locus in a family with mentally normal patientsM Mandl, R Caspari, A Jauch, et al.
Journal of Medical Genetics|August 3, 2000
Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsyB C Gohlke, K Haug, M Fukami, et al.
International Journal of Colorectal Disease|February 27, 2004
E-cadherin expression is homogeneously reduced in adenoma from patients with familial adenomatous polyposis: an immunohistochemical study of E-cadherin, beta-catenin and cyclooxygenase-2 expressionM Jungck, F Grünhage, U Spengler, et al.
Human Genetics|September 1, 1997
Loss of the PLA2G2A gene in a sporadic colorectal tumor of a patient with a PLA2G2A germline mutation and absence of PLA2G2A germline alterations in patients with FAPI Nimmrich, W Friedl, R Kruse, et al.
Human Genetics|March 1, 1993
Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1M Faiyaz ul Haque, S Uhlhaas, M Knapp, et al.
Journal of Medical Genetics|February 4, 2005
Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposisS Aretz, D Stienen, S Uhlhaas, et al.
Lung Cancer (Amsterdam, Netherlands)|January 11, 2005
Bronchioloalveolar carcinoma: a new cancer in Peutz-Jeghers syndromeA von Herbay, N Arens, W Friedl, et al.
Journal of Medical Genetics|July 6, 2004
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndromeE Mangold, C Pagenstecher, M Leister, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|October 6, 2005
[Detection of germline mutations in the APC gene with the protein truncation test]Xiao-Rong Liu, Xiang-Nian Shan, W Friedl, et al.
Pageof 20

Showing results (151-160 of 194) with videos related to

Sort By:
Pageof 20
Zeitschrift Fur Gastroenterologie|November 1, 1993
Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methodsR Caspari, W Friedl, T Böker, et al.
Human Genetics|February 1, 1996
Familial adenomatous polyposis: a submicroscopic deletion at the APC locus in a family with mentally normal patientsM Mandl, R Caspari, A Jauch, et al.
Journal of Medical Genetics|August 3, 2000
Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsyB C Gohlke, K Haug, M Fukami, et al.
International Journal of Colorectal Disease|February 27, 2004
E-cadherin expression is homogeneously reduced in adenoma from patients with familial adenomatous polyposis: an immunohistochemical study of E-cadherin, beta-catenin and cyclooxygenase-2 expressionM Jungck, F Grünhage, U Spengler, et al.
Human Genetics|September 1, 1997
Loss of the PLA2G2A gene in a sporadic colorectal tumor of a patient with a PLA2G2A germline mutation and absence of PLA2G2A germline alterations in patients with FAPI Nimmrich, W Friedl, R Kruse, et al.
Human Genetics|March 1, 1993
Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1M Faiyaz ul Haque, S Uhlhaas, M Knapp, et al.
Journal of Medical Genetics|February 4, 2005
Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposisS Aretz, D Stienen, S Uhlhaas, et al.
Lung Cancer (Amsterdam, Netherlands)|January 11, 2005
Bronchioloalveolar carcinoma: a new cancer in Peutz-Jeghers syndromeA von Herbay, N Arens, W Friedl, et al.
Journal of Medical Genetics|July 6, 2004
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndromeE Mangold, C Pagenstecher, M Leister, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|October 6, 2005
[Detection of germline mutations in the APC gene with the protein truncation test]Xiao-Rong Liu, Xiang-Nian Shan, W Friedl, et al.
Pageof 20