Search research articles
Contact Us
Filters
Showing results (11-20 of 143) with videos related to
Page
of 15
Sort By:
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-Welander
K Zerres, T Grimm
Human Genetics
|
January 1, 1983
Familial Robertsonian translocation t13q/15q
E Seidel, T Grimm
Neuropediatrics
|
August 1, 1986
Peroneal somatosensory evoked potentials in the "pure" form of hereditary spastic paraplegia
W 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 Database
J 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 analyses
B 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 families
C R Müller, T Grimm
Page
of 15
Search research articles
Search
Showing results (11-20 of 143) with videos related to
Sort By:
Page
of 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-Welander
K Zerres, T Grimm
Human Genetics
|
January 1, 1983
Familial Robertsonian translocation t13q/15q
E Seidel, T Grimm
Neuropediatrics
|
August 1, 1986
Peroneal somatosensory evoked potentials in the "pure" form of hereditary spastic paraplegia
W 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 Database
J 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 analyses
B 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 families
C R Müller, T Grimm
Page
of 15