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T Grimm

Showing results (11-20 of 143) with videos related to

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Deutsche Medizinische Wochenschrift (1946)|June 29, 1979
[The Bayes theorem in the differential diagnosis of ankylosing spondylitis (Bechterew)]T Grimm, U Langenbeck
Human Genetics|January 1, 1983
Genetic counseling in families with spinal muscular atrophy type Kugelberg-WelanderK Zerres, T Grimm
Human Genetics|January 1, 1983
Familial Robertsonian translocation t13q/15qE Seidel, T Grimm
Neuropediatrics|August 1, 1986
Peroneal somatosensory evoked potentials in the "pure" form of hereditary spastic paraplegiaW Görke, T Grimm
Deutsche Medizinische Wochenschrift (1946)|October 8, 1993
[Holt-Oram syndrome]F Kullmann, T Grimm
Zeitschrift Fur Kardiologie|March 1, 1980
[The genetic aspects of Williams-Beuren syndrome and the isolated form of the supravalvular aortic stenosis. Investigation of 128 families (author's transl)]T Grimm, H Wesselhoeft
Journal of Medical Genetics|August 1, 1987
A chromosome supplement to the London Dysmorphology DatabaseJ Brandl, T Grimm
Klinische Padiatrie|September 1, 1991
[Importance of germ cell mosaic for genetic counseling of families with Duchenne and Becker muscular dystrophy]M Janka, T Grimm
European Child & Adolescent Psychiatry|January 19, 2000
Linkage analysis and genetic models in dyslexia--considerations pertaining to discrete trait analysis and quantitative trait analysesB Müller-Myhsok, T Grimm
Human Genetics|October 1, 1986
Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy familiesC R Müller, T Grimm
Pageof 15

Showing results (11-20 of 143) with videos related to

Sort By:
Pageof 15
Deutsche Medizinische Wochenschrift (1946)|June 29, 1979
[The Bayes theorem in the differential diagnosis of ankylosing spondylitis (Bechterew)]T Grimm, U Langenbeck
Human Genetics|January 1, 1983
Genetic counseling in families with spinal muscular atrophy type Kugelberg-WelanderK Zerres, T Grimm
Human Genetics|January 1, 1983
Familial Robertsonian translocation t13q/15qE Seidel, T Grimm
Neuropediatrics|August 1, 1986
Peroneal somatosensory evoked potentials in the "pure" form of hereditary spastic paraplegiaW Görke, T Grimm
Deutsche Medizinische Wochenschrift (1946)|October 8, 1993
[Holt-Oram syndrome]F Kullmann, T Grimm
Zeitschrift Fur Kardiologie|March 1, 1980
[The genetic aspects of Williams-Beuren syndrome and the isolated form of the supravalvular aortic stenosis. Investigation of 128 families (author's transl)]T Grimm, H Wesselhoeft
Journal of Medical Genetics|August 1, 1987
A chromosome supplement to the London Dysmorphology DatabaseJ Brandl, T Grimm
Klinische Padiatrie|September 1, 1991
[Importance of germ cell mosaic for genetic counseling of families with Duchenne and Becker muscular dystrophy]M Janka, T Grimm
European Child & Adolescent Psychiatry|January 19, 2000
Linkage analysis and genetic models in dyslexia--considerations pertaining to discrete trait analysis and quantitative trait analysesB Müller-Myhsok, T Grimm
Human Genetics|October 1, 1986
Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy familiesC R Müller, T Grimm
Pageof 15