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

Marja W Wessels

Showing results (1-10 of 69) with videos related to

Pageof 7
Sort By:
Clinical Genetics|April 11, 2008
Mutations in sarcomeric protein genes not only lead to cardiomyopathy but also to congenital cardiovascular malformationsMarja W Wessels, Patrick J Willems
The New England Journal of Medicine|July 12, 2002
Images in clinical medicine. Chondrodysplasia punctataMarja W Wessels, Patrick J Willems
Prenatal Diagnosis|March 11, 2003
Mild fetal cerebral ventriculomegaly as a prenatal sonographic marker for Kartagener syndromeMarja W Wessels, Nicolette S den Hollander, Patrick J Willems
Clinical Dysmorphology|May 11, 2002
Kabuki syndrome: a review study of three hundred patientsMarja W Wessels, Alice S Brooks, Jeannette Hoogeboom, et al.
American Journal of Medical Genetics. Part A|May 31, 2008
Candidate gene analysis in three families with acilia syndromeMarja W Wessels, Avraham Avital, Mike Failly, et al.
American Journal of Medical Genetics. Part A|September 5, 2003
Prenatal diagnosis of boomerang dysplasiaMarja W Wessels, Nicolette S Den Hollander, Ronald R De Krijger, et al.
American Journal of Medical Genetics. Part A|June 10, 2003
Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata: case report and reviewMarja W Wessels, Nicolette J Den Hollander, Ronald R De Krijger, et al.
Molecular Syndromology|August 18, 2015
Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation FamilyJudith M A Verhagen, Nicole de Leeuw, Dimitri N M Papatsonis, et al.
Elife|July 23, 2025
Identification of novel human microcephaly-linked protein <i>Mtss2</i> that mediates cortical progenitor cell division and corticogenesis through <i>Nedd9-RhoA</i>Aurelie Carabalona, Henna Kallo, Maryanne Gonzalez, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 23, 2013
[Patients with aneurysms and osteoarthritis: Marfan syndrome ruled out, so what is it?]Denise van der Linde, Ingrid M B H van de Laar, Adriaan Moelker, et al.
Pageof 7

Showing results (1-10 of 69) with videos related to

Sort By:
Pageof 7
Clinical Genetics|April 11, 2008
Mutations in sarcomeric protein genes not only lead to cardiomyopathy but also to congenital cardiovascular malformationsMarja W Wessels, Patrick J Willems
The New England Journal of Medicine|July 12, 2002
Images in clinical medicine. Chondrodysplasia punctataMarja W Wessels, Patrick J Willems
Prenatal Diagnosis|March 11, 2003
Mild fetal cerebral ventriculomegaly as a prenatal sonographic marker for Kartagener syndromeMarja W Wessels, Nicolette S den Hollander, Patrick J Willems
Clinical Dysmorphology|May 11, 2002
Kabuki syndrome: a review study of three hundred patientsMarja W Wessels, Alice S Brooks, Jeannette Hoogeboom, et al.
American Journal of Medical Genetics. Part A|May 31, 2008
Candidate gene analysis in three families with acilia syndromeMarja W Wessels, Avraham Avital, Mike Failly, et al.
American Journal of Medical Genetics. Part A|September 5, 2003
Prenatal diagnosis of boomerang dysplasiaMarja W Wessels, Nicolette S Den Hollander, Ronald R De Krijger, et al.
American Journal of Medical Genetics. Part A|June 10, 2003
Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata: case report and reviewMarja W Wessels, Nicolette J Den Hollander, Ronald R De Krijger, et al.
Molecular Syndromology|August 18, 2015
Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation FamilyJudith M A Verhagen, Nicole de Leeuw, Dimitri N M Papatsonis, et al.
Elife|July 23, 2025
Identification of novel human microcephaly-linked protein <i>Mtss2</i> that mediates cortical progenitor cell division and corticogenesis through <i>Nedd9-RhoA</i>Aurelie Carabalona, Henna Kallo, Maryanne Gonzalez, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 23, 2013
[Patients with aneurysms and osteoarthritis: Marfan syndrome ruled out, so what is it?]Denise van der Linde, Ingrid M B H van de Laar, Adriaan Moelker, et al.
Pageof 7