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Investigative Ophthalmology & Visual Science
|
October 3, 2001
Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene
H P Scholl, H Langrová, C M Pusch, et al.
The Science of the Total Environment
|
January 31, 2012
Graveyards - special landfills
S Fiedler, J Breuer, C M Pusch, et al.
Human Genetics
|
September 12, 2000
Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1
F K Jacobi, M Broghammer, K Pesch, et al.
International Journal of Paleopathology
|
March 15, 2018
Eleonora of Toledo (1522-1562): Evidence for tuberculosis and leishmaniasis co-infection in Renaissance Italy
R Bianucci, V Giuffra, B E Bachmeier, et al.
Investigative Ophthalmology & Visual Science
|
May 1, 2001
Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy
F K Jacobi, B Leo-Kottler, K Mittelviefhaus, et al.
Neurobiology of Disease
|
July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness
F Mirghomizadeh, M Pfister, F Apaydin, et al.
International Journal of Molecular Medicine
|
June 16, 2001
Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders
K Pesch, J Tomiuk, M Broghammer, et al.
American Journal of Human Genetics
|
May 2, 2000
Genomic differentiation of Neanderthals and anatomically modern man allows a fossil-DNA-based classification of morphologically indistinguishable hominid bones
M Scholz, L Bachmann, G J Nicholson, et al.
Molecular Biology and Evolution
|
July 16, 2004
PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutations
C M Pusch, M Broghammer, G J Nicholson, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
March 26, 2004
Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33
C M Pusch, B Meyer, S Kupka, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Investigative Ophthalmology & Visual Science
|
October 3, 2001
Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene
H P Scholl, H Langrová, C M Pusch, et al.
The Science of the Total Environment
|
January 31, 2012
Graveyards - special landfills
S Fiedler, J Breuer, C M Pusch, et al.
Human Genetics
|
September 12, 2000
Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1
F K Jacobi, M Broghammer, K Pesch, et al.
International Journal of Paleopathology
|
March 15, 2018
Eleonora of Toledo (1522-1562): Evidence for tuberculosis and leishmaniasis co-infection in Renaissance Italy
R Bianucci, V Giuffra, B E Bachmeier, et al.
Investigative Ophthalmology & Visual Science
|
May 1, 2001
Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy
F K Jacobi, B Leo-Kottler, K Mittelviefhaus, et al.
Neurobiology of Disease
|
July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness
F Mirghomizadeh, M Pfister, F Apaydin, et al.
International Journal of Molecular Medicine
|
June 16, 2001
Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders
K Pesch, J Tomiuk, M Broghammer, et al.
American Journal of Human Genetics
|
May 2, 2000
Genomic differentiation of Neanderthals and anatomically modern man allows a fossil-DNA-based classification of morphologically indistinguishable hominid bones
M Scholz, L Bachmann, G J Nicholson, et al.
Molecular Biology and Evolution
|
July 16, 2004
PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutations
C M Pusch, M Broghammer, G J Nicholson, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
March 26, 2004
Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33
C M Pusch, B Meyer, S Kupka, et al.
Page
of 4