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Zeitschrift Fur Rheumatologie
|
January 26, 2011
[The genetics of vasculitides]
J U Holle, S Wieczorek, J T Epplen, et al.
Journal of the International Federation of Clinical Chemistry
|
May 8, 1994
Molecular biology techniques in the diagnosis of monogenic diseases
C Wagener, J T Epplen, H Ehrlich, et al.
Chromosoma
|
November 1, 1979
Contrasting DNA sequence organisation patterns in sauropsidian genomes
J T Epplen, U Diedrich, M Wagenmann, et al.
Zeitschrift Fur Gastroenterologie
|
July 8, 2005
[Evaluation of outpatient management in HNPCC]
K Bach, D Hüppe, W Schmiegel, et al.
Human Genetics
|
February 1, 1997
Transmission distortion of the mutant alleles in spinocerebellar ataxia
O Riess, J T Epplen, G Amoiridis, et al.
Psychiatric Genetics
|
April 20, 2004
A rare form of narcolepsy (HLA-DR2-) shows possible association with (functionally relevant) alpha-interferon gene polymorphisms
S Wieczorek, N Dahmen, M Kasten, et al.
Human Genetics
|
July 1, 1990
Heterogeneities in the distribution of (GACA)n simple repeats in the karyotypes of primates and mouse
I Nanda, C Deubelbeiss, M Guttenbach, et al.
Proceedings. Biological Sciences
|
June 25, 1999
DNA analyses support the hypothesis that infanticide is adaptive in langur monkeys
C Borries, K Launhardt, C Epplen, et al.
Epilepsy Research
|
March 27, 1999
Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel (hKCa3) and susceptibility to idiopathic generalized epilepsy
T Sander, L Schölz, D Janz, et al.
Electrophoresis
|
May 1, 1995
Indirect DNA/gene diagnoses via electrophoresis--an obsolete principle?
J T Epplen, J Buitkamp, C Epplen, et al.
Page
of 37
Search research articles
Search
Showing results (141-150 of 365) with videos related to
Sort By:
Page
of 37
Zeitschrift Fur Rheumatologie
|
January 26, 2011
[The genetics of vasculitides]
J U Holle, S Wieczorek, J T Epplen, et al.
Journal of the International Federation of Clinical Chemistry
|
May 8, 1994
Molecular biology techniques in the diagnosis of monogenic diseases
C Wagener, J T Epplen, H Ehrlich, et al.
Chromosoma
|
November 1, 1979
Contrasting DNA sequence organisation patterns in sauropsidian genomes
J T Epplen, U Diedrich, M Wagenmann, et al.
Zeitschrift Fur Gastroenterologie
|
July 8, 2005
[Evaluation of outpatient management in HNPCC]
K Bach, D Hüppe, W Schmiegel, et al.
Human Genetics
|
February 1, 1997
Transmission distortion of the mutant alleles in spinocerebellar ataxia
O Riess, J T Epplen, G Amoiridis, et al.
Psychiatric Genetics
|
April 20, 2004
A rare form of narcolepsy (HLA-DR2-) shows possible association with (functionally relevant) alpha-interferon gene polymorphisms
S Wieczorek, N Dahmen, M Kasten, et al.
Human Genetics
|
July 1, 1990
Heterogeneities in the distribution of (GACA)n simple repeats in the karyotypes of primates and mouse
I Nanda, C Deubelbeiss, M Guttenbach, et al.
Proceedings. Biological Sciences
|
June 25, 1999
DNA analyses support the hypothesis that infanticide is adaptive in langur monkeys
C Borries, K Launhardt, C Epplen, et al.
Epilepsy Research
|
March 27, 1999
Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel (hKCa3) and susceptibility to idiopathic generalized epilepsy
T Sander, L Schölz, D Janz, et al.
Electrophoresis
|
May 1, 1995
Indirect DNA/gene diagnoses via electrophoresis--an obsolete principle?
J T Epplen, J Buitkamp, C Epplen, et al.
Page
of 37