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T Grimm

Showing results (81-90 of 143) with videos related to

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Klinische Padiatrie|May 1, 1993
[Holt-Oram syndrome in combination with reciprocal translocation, lung hypoplasia and cardiomyopathy]F Kullmann, R Koch, W Feichtinger, et al.
Annals of Human Genetics|April 22, 2006
Modelling germline mosaicism and different new mutation rates simultaneously for appropriate risk calculations in families with Duchenne muscular dystrophyC Fischer, W Gross, J Krüger, et al.
Der Urologe. Ausg. A|August 13, 2016
[Non-muscle invasive bladder cancer : Current aspects of diagnostics, local therapy options and the update of the 2016 WHO classification]A Karl, T Grimm, F Jokisch, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|December 5, 1997
Preparing residents for managed care practice using an experience-based curriculumA G Gomez, C T Grimm, E F Yee, et al.
Applied Microbiology and Biotechnology|January 20, 2012
Enzyme-based glucose delivery as a high content screening tool in yeast-based whole-cell biocatalysisT Grimm, M Grimm, R Klat, et al.
Der Urologe. Ausg. A|March 3, 2019
[Active surveillance of prostate cancer : An update]M Chaloupka, T Westhofen, A Kretschmer, et al.
American Journal of Human Genetics|July 1, 1977
Evidence for preferential X-chromosome inactivation in a family with Fabry diseaseH H Ropers, T F Wienker, T Grimm, et al.
Journal of Medical Genetics|December 1, 1995
Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familesI Stec, W Kress, G Meng, et al.
Human Genetics|March 1, 1993
Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigreeA Sander, H Moser, S Liechti-Gallati, et al.
Journal of Clinical Periodontology|December 22, 1999
Interleukin-1 haplotype and periodontal disease progression following therapyB Ehmke, W Kress, H Karch, et al.
Pageof 15

Showing results (81-90 of 143) with videos related to

Sort By:
Pageof 15
Klinische Padiatrie|May 1, 1993
[Holt-Oram syndrome in combination with reciprocal translocation, lung hypoplasia and cardiomyopathy]F Kullmann, R Koch, W Feichtinger, et al.
Annals of Human Genetics|April 22, 2006
Modelling germline mosaicism and different new mutation rates simultaneously for appropriate risk calculations in families with Duchenne muscular dystrophyC Fischer, W Gross, J Krüger, et al.
Der Urologe. Ausg. A|August 13, 2016
[Non-muscle invasive bladder cancer : Current aspects of diagnostics, local therapy options and the update of the 2016 WHO classification]A Karl, T Grimm, F Jokisch, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|December 5, 1997
Preparing residents for managed care practice using an experience-based curriculumA G Gomez, C T Grimm, E F Yee, et al.
Applied Microbiology and Biotechnology|January 20, 2012
Enzyme-based glucose delivery as a high content screening tool in yeast-based whole-cell biocatalysisT Grimm, M Grimm, R Klat, et al.
Der Urologe. Ausg. A|March 3, 2019
[Active surveillance of prostate cancer : An update]M Chaloupka, T Westhofen, A Kretschmer, et al.
American Journal of Human Genetics|July 1, 1977
Evidence for preferential X-chromosome inactivation in a family with Fabry diseaseH H Ropers, T F Wienker, T Grimm, et al.
Journal of Medical Genetics|December 1, 1995
Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familesI Stec, W Kress, G Meng, et al.
Human Genetics|March 1, 1993
Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigreeA Sander, H Moser, S Liechti-Gallati, et al.
Journal of Clinical Periodontology|December 22, 1999
Interleukin-1 haplotype and periodontal disease progression following therapyB Ehmke, W Kress, H Karch, et al.
Pageof 15