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Proceedings of the National Academy of Sciences of the United States of America
|
April 2, 1996
Mammalian ubiquitin-conjugating enzyme Ubc9 interacts with Rad51 recombination protein and localizes in synaptonemal complexes
O V Kovalenko, A W Plug, T Haaf, et al.
Journal of Medical Genetics
|
April 6, 2001
Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome
G Borck, J Wirth, T Hardt, et al.
Cytogenetic and Genome Research
|
February 23, 2013
The hemiphractid frogs. Phylogeny, embryology, life history, and cytogenetics
M Schmid, C Steinlein, J P Bogart, et al.
Molecular Syndromology
|
February 20, 2014
Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss
B Vona, C Neuner, N El Hajj, et al.
The American Journal of Pathology
|
March 7, 2013
The 140-kD isoform of CD56 (NCAM1) directs the molecular pathogenesis of ischemic cardiomyopathy
Mehmet Kemal Tur, Benjamin Etschmann, Alexander Benz, et al.
Clinical Genetics
|
May 27, 2015
DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics
B Vona, M A H Hofrichter, C Neuner, et al.
Genomics
|
September 7, 2001
Genomic organization and expression of the doublesex-related gene cluster in vertebrates and detection of putative regulatory regions for DMRT1
B Brunner, U Hornung, Z Shan, et al.
Neurology
|
July 23, 2003
D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detection
R J L F Lemmers, M Osborn, T Haaf, et al.
Journal of Medical Genetics
|
May 5, 1999
Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes
J Wirth, H G Nothwang, S van der Maarel, et al.
Cytogenetic and Genome Research
|
March 30, 2012
Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate cortices
E Schneider, S Mayer, N El Hajj, et al.
Page
of 17
Search research articles
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Showing results (151-160 of 170) with videos related to
Sort By:
Page
of 17
Proceedings of the National Academy of Sciences of the United States of America
|
April 2, 1996
Mammalian ubiquitin-conjugating enzyme Ubc9 interacts with Rad51 recombination protein and localizes in synaptonemal complexes
O V Kovalenko, A W Plug, T Haaf, et al.
Journal of Medical Genetics
|
April 6, 2001
Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome
G Borck, J Wirth, T Hardt, et al.
Cytogenetic and Genome Research
|
February 23, 2013
The hemiphractid frogs. Phylogeny, embryology, life history, and cytogenetics
M Schmid, C Steinlein, J P Bogart, et al.
Molecular Syndromology
|
February 20, 2014
Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss
B Vona, C Neuner, N El Hajj, et al.
The American Journal of Pathology
|
March 7, 2013
The 140-kD isoform of CD56 (NCAM1) directs the molecular pathogenesis of ischemic cardiomyopathy
Mehmet Kemal Tur, Benjamin Etschmann, Alexander Benz, et al.
Clinical Genetics
|
May 27, 2015
DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics
B Vona, M A H Hofrichter, C Neuner, et al.
Genomics
|
September 7, 2001
Genomic organization and expression of the doublesex-related gene cluster in vertebrates and detection of putative regulatory regions for DMRT1
B Brunner, U Hornung, Z Shan, et al.
Neurology
|
July 23, 2003
D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detection
R J L F Lemmers, M Osborn, T Haaf, et al.
Journal of Medical Genetics
|
May 5, 1999
Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes
J Wirth, H G Nothwang, S van der Maarel, et al.
Cytogenetic and Genome Research
|
March 30, 2012
Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate cortices
E Schneider, S Mayer, N El Hajj, et al.
Page
of 17