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Chromosoma
|
December 6, 1978
DNA sequence organisation in avian genomes
J T Epplen, M Leipoldt, W Engel, et al.
Cytogenetic and Genome Research
|
March 9, 2004
The application of region-specific probes for the resolution of duplication 8p: a case report and a review of the literature
B Pabst, M Arslan-Kirchner, J Schmidtke, et al.
Human Genetics
|
February 1, 1991
Physical mapping of two Xp markers DXS16 and DXS143
U Thies, V V Rao, W Engel, et al.
The Journal of Physical Chemistry. A
|
July 13, 2006
Probing excited-state dynamics and intramolecular proton transfer in 1-acylaminoanthraquinones via the intermolecular solvent response
Sarah J Schmidtke, David F Underwood, David A Blank
Human Genetics
|
November 1, 1992
A termination mutation (2143delT) in the CFTR gene of German cystic fibrosis patients
T Dörk, N Kälin, M Stuhrmann, et al.
Human Genetics
|
January 1, 1981
Characterization of a new aberration of the human Y chromosome by banding methods and DNA restriction endonuclease analysis
M Schmid, H Gall, W Schempp, et al.
Human Genetics
|
January 1, 1987
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers
E Wilichowski, M Krawczak, E Seemanova, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
May 1, 1997
Conserved Y-chromosomal location of TSPY in Bovidae
T Vogel, S Borgmann, F Dechend, et al.
Human Mutation
|
January 1, 1992
Missense variation of the CFTR gene codon 507
K Will, M Stuhrmann, H Ellemunter, et al.
Cytogenetics and Cell Genetics
|
February 15, 2001
Molecular evolution of the murine tspy genes
S Schubert, F Dechend, B Skawran, et al.
Page
of 22
Search research articles
Search
Showing results (101-110 of 214) with videos related to
Sort By:
Page
of 22
Chromosoma
|
December 6, 1978
DNA sequence organisation in avian genomes
J T Epplen, M Leipoldt, W Engel, et al.
Cytogenetic and Genome Research
|
March 9, 2004
The application of region-specific probes for the resolution of duplication 8p: a case report and a review of the literature
B Pabst, M Arslan-Kirchner, J Schmidtke, et al.
Human Genetics
|
February 1, 1991
Physical mapping of two Xp markers DXS16 and DXS143
U Thies, V V Rao, W Engel, et al.
The Journal of Physical Chemistry. A
|
July 13, 2006
Probing excited-state dynamics and intramolecular proton transfer in 1-acylaminoanthraquinones via the intermolecular solvent response
Sarah J Schmidtke, David F Underwood, David A Blank
Human Genetics
|
November 1, 1992
A termination mutation (2143delT) in the CFTR gene of German cystic fibrosis patients
T Dörk, N Kälin, M Stuhrmann, et al.
Human Genetics
|
January 1, 1981
Characterization of a new aberration of the human Y chromosome by banding methods and DNA restriction endonuclease analysis
M Schmid, H Gall, W Schempp, et al.
Human Genetics
|
January 1, 1987
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers
E Wilichowski, M Krawczak, E Seemanova, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
May 1, 1997
Conserved Y-chromosomal location of TSPY in Bovidae
T Vogel, S Borgmann, F Dechend, et al.
Human Mutation
|
January 1, 1992
Missense variation of the CFTR gene codon 507
K Will, M Stuhrmann, H Ellemunter, et al.
Cytogenetics and Cell Genetics
|
February 15, 2001
Molecular evolution of the murine tspy genes
S Schubert, F Dechend, B Skawran, et al.
Page
of 22