Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Martijn H Breuning

Showing results (81-90 of 112) with videos related to

Pageof 12
Sort By:
Psycho-Oncology|July 10, 2008
Genetic testing in familial melanoma: uptake and implicationsFemke A de Snoo, Samantha R Riedijk, Anneke M van Mil, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristicsOmer T Njajou, Gerard de Jong, Bianca Berghuis, et al.
Journal of the American Academy of Dermatology|February 6, 2007
From sporadic atypical nevi to familial melanoma: risk analysis for melanoma in sporadic atypical nevus patientsFemke A de Snoo, Marije W Kroon, Wilma Bergman, et al.
Acta Neuropathologica|May 21, 2003
Evaluation of diagnostic NOTCH3 immunostaining in CADASILSaskia A J Lesnik Oberstein, Sjoerd G van Duinen, Rivka van den Boom, et al.
The Journal of Clinical Endocrinology and Metabolism|June 22, 2006
Clinical and biochemical characteristics of a male patient with a novel homozygous STAT5b mutationSolrun Vidarsdottir, Marie J E Walenkamp, Alberto M Pereira, et al.
Journal of the American Society of Nephrology : JASN|March 30, 2016
Inhibition of Activin Signaling Slows Progression of Polycystic Kidney DiseaseWouter N Leonhard, Steven J Kunnen, Anna J Plugge, et al.
European Journal of Human Genetics : EJHG|May 14, 2009
A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays firstAntoinet C J Gijsbers, Janet Y K Lew, Cathy A J Bosch, et al.
Human Genetics|October 28, 2008
Identification of copy number variants associated with BPES-like phenotypesAntoinet C J Gijsbers, Barbara D'haene, Yvonne Hilhorst-Hofstee, et al.
European Journal of Human Genetics : EJHG|November 11, 2010
The clinical spectrum of complete FBN1 allele deletionsYvonne Hilhorst-Hofstee, Ben C J Hamel, Joke B G M Verheij, et al.
Plos One|May 11, 2012
Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriersKai Hang Yiu, Douwe E Atsma, Victoria Delgado, et al.
Pageof 12

Showing results (81-90 of 112) with videos related to

Sort By:
Pageof 12
Psycho-Oncology|July 10, 2008
Genetic testing in familial melanoma: uptake and implicationsFemke A de Snoo, Samantha R Riedijk, Anneke M van Mil, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristicsOmer T Njajou, Gerard de Jong, Bianca Berghuis, et al.
Journal of the American Academy of Dermatology|February 6, 2007
From sporadic atypical nevi to familial melanoma: risk analysis for melanoma in sporadic atypical nevus patientsFemke A de Snoo, Marije W Kroon, Wilma Bergman, et al.
Acta Neuropathologica|May 21, 2003
Evaluation of diagnostic NOTCH3 immunostaining in CADASILSaskia A J Lesnik Oberstein, Sjoerd G van Duinen, Rivka van den Boom, et al.
The Journal of Clinical Endocrinology and Metabolism|June 22, 2006
Clinical and biochemical characteristics of a male patient with a novel homozygous STAT5b mutationSolrun Vidarsdottir, Marie J E Walenkamp, Alberto M Pereira, et al.
Journal of the American Society of Nephrology : JASN|March 30, 2016
Inhibition of Activin Signaling Slows Progression of Polycystic Kidney DiseaseWouter N Leonhard, Steven J Kunnen, Anna J Plugge, et al.
European Journal of Human Genetics : EJHG|May 14, 2009
A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays firstAntoinet C J Gijsbers, Janet Y K Lew, Cathy A J Bosch, et al.
Human Genetics|October 28, 2008
Identification of copy number variants associated with BPES-like phenotypesAntoinet C J Gijsbers, Barbara D'haene, Yvonne Hilhorst-Hofstee, et al.
European Journal of Human Genetics : EJHG|November 11, 2010
The clinical spectrum of complete FBN1 allele deletionsYvonne Hilhorst-Hofstee, Ben C J Hamel, Joke B G M Verheij, et al.
Plos One|May 11, 2012
Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriersKai Hang Yiu, Douwe E Atsma, Victoria Delgado, et al.
Pageof 12