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Breuning

Showing results (261-270 of 391) with videos related to

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American Journal of Medical Genetics|September 13, 2000
Recurrent digital fibroma, focal dermal hypoplasia, and limb malformationsM H Breuning, A P Oranje, R A Langemeijer, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 28, 2007
Pathogenic sequence for dissecting aneurysm formation in a hypomorphic polycystic kidney disease 1 mouse modelSabrine Hassane, Nanna Claij, Irma S Lantinga-van Leeuwen, et al.
Human Molecular Genetics|April 30, 2009
Toxic tubular injury in kidneys from Pkd1-deletion mice accelerates cystogenesis accompanied by dysregulated planar cell polarity and canonical Wnt signaling pathwaysHester Happé, Wouter N Leonhard, Annemieke van der Wal, et al.
Neurology|September 26, 2001
Cerebral microbleeds in CADASILS A Lesnik Oberstein, R van den Boom, M A van Buchem, et al.
American Journal of Human Genetics|July 12, 2002
Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridizationStefan White, Margot Kalf, Qiang Liu, et al.
Human Genetics|March 23, 2007
Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3Mark B Consugar, Vickie J Kubly, Donna J Lager, et al.
Genomics|September 15, 1994
A large duplicated area in the polycystic kidney disease 1 (PKD1) region of chromosome 16 is prone to rearrangementP C Harris, S Thomas, A B MacCarthy, et al.
European Journal of Human Genetics : EJHG|July 21, 2005
Deletion and duplication screening in the DMD gene using MLPATanja Lalic, Rolf H A M Vossen, Jordy Coffa, et al.
Cytogenetic and Genome Research|March 17, 2009
Methods to detect CNVs in the human genomeE Aten, S J White, M E Kalf, et al.
European Journal of Human Genetics : EJHG|June 7, 2012
An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophyApollonia T J M Helderman-van den Enden, Kamlesh Madan, Martijn H Breuning, et al.
Pageof 40

Showing results (261-270 of 391) with videos related to

Sort By:
Pageof 40
American Journal of Medical Genetics|September 13, 2000
Recurrent digital fibroma, focal dermal hypoplasia, and limb malformationsM H Breuning, A P Oranje, R A Langemeijer, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 28, 2007
Pathogenic sequence for dissecting aneurysm formation in a hypomorphic polycystic kidney disease 1 mouse modelSabrine Hassane, Nanna Claij, Irma S Lantinga-van Leeuwen, et al.
Human Molecular Genetics|April 30, 2009
Toxic tubular injury in kidneys from Pkd1-deletion mice accelerates cystogenesis accompanied by dysregulated planar cell polarity and canonical Wnt signaling pathwaysHester Happé, Wouter N Leonhard, Annemieke van der Wal, et al.
Neurology|September 26, 2001
Cerebral microbleeds in CADASILS A Lesnik Oberstein, R van den Boom, M A van Buchem, et al.
American Journal of Human Genetics|July 12, 2002
Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridizationStefan White, Margot Kalf, Qiang Liu, et al.
Human Genetics|March 23, 2007
Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3Mark B Consugar, Vickie J Kubly, Donna J Lager, et al.
Genomics|September 15, 1994
A large duplicated area in the polycystic kidney disease 1 (PKD1) region of chromosome 16 is prone to rearrangementP C Harris, S Thomas, A B MacCarthy, et al.
European Journal of Human Genetics : EJHG|July 21, 2005
Deletion and duplication screening in the DMD gene using MLPATanja Lalic, Rolf H A M Vossen, Jordy Coffa, et al.
Cytogenetic and Genome Research|March 17, 2009
Methods to detect CNVs in the human genomeE Aten, S J White, M E Kalf, et al.
European Journal of Human Genetics : EJHG|June 7, 2012
An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophyApollonia T J M Helderman-van den Enden, Kamlesh Madan, Martijn H Breuning, et al.
Pageof 40