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T Grimm

Showing results (71-80 of 143) with videos related to

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American Journal of Diseases of Children (1960)|December 1, 1993
X-linked lymphoproliferative disease. Detection of a paternally inherited mutation in a German family using haplotype analysisV Schuster, W Kress, W Friedrich, et al.
Journal of Clinical Pathology|October 6, 2006
Expression of calcitonin receptor-like receptor in human vascular tumoursS Hagner, U Stahl, T Grimm, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 27, 1998
[Linear and whorled nevoid hypermelanosis. Case report and review of the literature]U Hofmann, N Wagner, T Grimm, et al.
General and Comparative Endocrinology|June 10, 2011
Higher thyroid hormone receptor expression correlates with short larval periods in spadefoot toads and increases metamorphic rateAmy R Hollar, Jinyoung Choi, Adam T Grimm, et al.
Urology|July 1, 1992
Solitary cerebellar metastasis from transitional cell carcinoma of bladderG J Shamdas, G D McLaren, T Grimm, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Parental source effect on inherited mutations in the dystrophin gene of mice and humansW Kress, T Grimm, C R Müller, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM)C Schneider, T Grimm, W Kress, et al.
Neuromuscular Disorders : NMD|June 19, 2001
Proximal myotonic myopathy and proximal myotonic dystrophy: two different entities? The phenotypic variability of proximal myotonic syndromesC Schneider, C Wessig, C R Müller, et al.
Human Genetics|July 1, 1988
The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type IIE M Westphal, E Natt, T Grimm, et al.
CBE Life Sciences Education|August 26, 2025
Longitudinal Study of the FIRST IV Program: Biology Departments' Influence on TeachingDiane Ebert-May, Jessica Middlemis Maher, Lucas B Hill, et al.
Pageof 15

Showing results (71-80 of 143) with videos related to

Sort By:
Pageof 15
American Journal of Diseases of Children (1960)|December 1, 1993
X-linked lymphoproliferative disease. Detection of a paternally inherited mutation in a German family using haplotype analysisV Schuster, W Kress, W Friedrich, et al.
Journal of Clinical Pathology|October 6, 2006
Expression of calcitonin receptor-like receptor in human vascular tumoursS Hagner, U Stahl, T Grimm, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 27, 1998
[Linear and whorled nevoid hypermelanosis. Case report and review of the literature]U Hofmann, N Wagner, T Grimm, et al.
General and Comparative Endocrinology|June 10, 2011
Higher thyroid hormone receptor expression correlates with short larval periods in spadefoot toads and increases metamorphic rateAmy R Hollar, Jinyoung Choi, Adam T Grimm, et al.
Urology|July 1, 1992
Solitary cerebellar metastasis from transitional cell carcinoma of bladderG J Shamdas, G D McLaren, T Grimm, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Parental source effect on inherited mutations in the dystrophin gene of mice and humansW Kress, T Grimm, C R Müller, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM)C Schneider, T Grimm, W Kress, et al.
Neuromuscular Disorders : NMD|June 19, 2001
Proximal myotonic myopathy and proximal myotonic dystrophy: two different entities? The phenotypic variability of proximal myotonic syndromesC Schneider, C Wessig, C R Müller, et al.
Human Genetics|July 1, 1988
The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type IIE M Westphal, E Natt, T Grimm, et al.
CBE Life Sciences Education|August 26, 2025
Longitudinal Study of the FIRST IV Program: Biology Departments' Influence on TeachingDiane Ebert-May, Jessica Middlemis Maher, Lucas B Hill, et al.
Pageof 15