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W Friedl

Showing results (161-170 of 194) with videos related to

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The American Journal of Dermatopathology|October 27, 1999
Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic studyA Rütten, W Burgdorf, H Hügel, et al.
The Journal of Pathology|November 2, 2007
Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndromeN Rahner, N Friedrichs, V Steinke, et al.
Human Genetics|November 1, 1986
The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patientsP Propping, W Friedl, M Huschka, et al.
The Journal of Investigative Dermatology|March 7, 2001
"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivationR Kruse, A Rütten, H R Hosseiny-Malayeri, et al.
Microsurgery|January 1, 1996
Technetium-99m human immunoglobulin (HIG): a new substance for scintigraphic detection of bone and joint infectionsH G Machens, N Pallua, M Becker, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 19, 2011
"Crowned" univalent indium complexes as donors? Experimental and computational insights on the valence isomers of EE'X4 speciesBenjamin F T Cooper, Hiyam Hamaed, Warren W Friedl, et al.
Human Molecular Genetics|March 1, 1995
Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444R Caspari, S Olschwang, W Friedl, et al.
Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry|September 20, 2016
<sup>14</sup> N Solid-State NMR Spectroscopy of Amino AcidsStanislav L Veinberg, Zachary W Friedl, Austin W Lindquist, et al.
Neoplasma|October 24, 2000
Approaches to identification of HNPCC suspected patients in Slovak populationI Fridrichová, D Ilencíková, W Friedl, et al.
International Journal of Molecular Medicine|December 16, 1998
Mosaicism for Charcot-Marie-Tooth disease type 1A: onset in childhood suggests somatic reversion in early developmental stagesB Rautenstrauss, T Liehr, C Fuchs, et al.
Pageof 20

Showing results (161-170 of 194) with videos related to

Sort By:
Pageof 20
The American Journal of Dermatopathology|October 27, 1999
Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic studyA Rütten, W Burgdorf, H Hügel, et al.
The Journal of Pathology|November 2, 2007
Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndromeN Rahner, N Friedrichs, V Steinke, et al.
Human Genetics|November 1, 1986
The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patientsP Propping, W Friedl, M Huschka, et al.
The Journal of Investigative Dermatology|March 7, 2001
"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivationR Kruse, A Rütten, H R Hosseiny-Malayeri, et al.
Microsurgery|January 1, 1996
Technetium-99m human immunoglobulin (HIG): a new substance for scintigraphic detection of bone and joint infectionsH G Machens, N Pallua, M Becker, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 19, 2011
"Crowned" univalent indium complexes as donors? Experimental and computational insights on the valence isomers of EE'X4 speciesBenjamin F T Cooper, Hiyam Hamaed, Warren W Friedl, et al.
Human Molecular Genetics|March 1, 1995
Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444R Caspari, S Olschwang, W Friedl, et al.
Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry|September 20, 2016
<sup>14</sup> N Solid-State NMR Spectroscopy of Amino AcidsStanislav L Veinberg, Zachary W Friedl, Austin W Lindquist, et al.
Neoplasma|October 24, 2000
Approaches to identification of HNPCC suspected patients in Slovak populationI Fridrichová, D Ilencíková, W Friedl, et al.
International Journal of Molecular Medicine|December 16, 1998
Mosaicism for Charcot-Marie-Tooth disease type 1A: onset in childhood suggests somatic reversion in early developmental stagesB Rautenstrauss, T Liehr, C Fuchs, et al.
Pageof 20