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Carlo L M Marcelis

Showing results (1-10 of 36) with videos related to

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Clinical Dysmorphology|June 1, 2013
A rare complex malformation of the hand in split hand foot malformation type 3 (SHFM3)Charlotte W Ockeloen, Jan M Cobben, Carlo L M Marcelis, et al.
European Journal of Human Genetics : EJHG|March 29, 2012
Unravelling fears of genetic discrimination: an exploratory study of Dutch HCM families in an era of genetic non-discrimination actsEls Geelen, Klasien Horstman, Carlo L M Marcelis, et al.
American Journal of Medical Genetics. Part A|July 9, 2011
Constructing "best interests": genetic testing of children in families with hypertrophic cardiomyopathyEls Geelen, Ine Van Hoyweghen, Pieter A Doevendans, et al.
Journal of Pediatric Surgery|August 6, 2005
The Currarino triad: the variable expressionPieter J Emans, Gauke Kootstra, Carlo L M Marcelis, et al.
Birth Defects Research. Part C, Embryo Today : Reviews|December 30, 2014
Genetic and nongenetic etiology of nonsyndromic anorectal malformations: a systematic reviewCharlotte H W Wijers, Iris A L M van Rooij, Carlo L M Marcelis, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 18, 2015
When is a post-mortem skeletal survey of the fetus indicated, and when not?Karin Kamphuis-van Ulzen, Desirée H J L M Koopmanschap, Carlo L M Marcelis, et al.
European Journal of Pediatrics|October 27, 2015
Patients with anorectal malformation and upper limb anomalies: genetic evaluation is warrantedDesiree van den Hondel, Charlotte H W Wijers, Yolande van Bever, et al.
The International Journal of Cardiovascular Imaging|October 25, 2017
High T2-weighted signal intensity for risk prediction of sudden cardiac death in hypertrophic cardiomyopathyD H Frank Gommans, G Etienne Cramer, Jeannette Bakker, et al.
Human Mutation|May 13, 2008
Genotype-phenotype correlations in MYCN-related Feingold syndromeCarlo L M Marcelis, Frans A Hol, Gail E Graham, et al.
Journal of Pediatric Surgery|December 10, 2013
First results of a European multi-center registry of patients with anorectal malformationsIvo de Blaauw, Charlotte H W Wijers, Eberhard Schmiedeke, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Clinical Dysmorphology|June 1, 2013
A rare complex malformation of the hand in split hand foot malformation type 3 (SHFM3)Charlotte W Ockeloen, Jan M Cobben, Carlo L M Marcelis, et al.
European Journal of Human Genetics : EJHG|March 29, 2012
Unravelling fears of genetic discrimination: an exploratory study of Dutch HCM families in an era of genetic non-discrimination actsEls Geelen, Klasien Horstman, Carlo L M Marcelis, et al.
American Journal of Medical Genetics. Part A|July 9, 2011
Constructing "best interests": genetic testing of children in families with hypertrophic cardiomyopathyEls Geelen, Ine Van Hoyweghen, Pieter A Doevendans, et al.
Journal of Pediatric Surgery|August 6, 2005
The Currarino triad: the variable expressionPieter J Emans, Gauke Kootstra, Carlo L M Marcelis, et al.
Birth Defects Research. Part C, Embryo Today : Reviews|December 30, 2014
Genetic and nongenetic etiology of nonsyndromic anorectal malformations: a systematic reviewCharlotte H W Wijers, Iris A L M van Rooij, Carlo L M Marcelis, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 18, 2015
When is a post-mortem skeletal survey of the fetus indicated, and when not?Karin Kamphuis-van Ulzen, Desirée H J L M Koopmanschap, Carlo L M Marcelis, et al.
European Journal of Pediatrics|October 27, 2015
Patients with anorectal malformation and upper limb anomalies: genetic evaluation is warrantedDesiree van den Hondel, Charlotte H W Wijers, Yolande van Bever, et al.
The International Journal of Cardiovascular Imaging|October 25, 2017
High T2-weighted signal intensity for risk prediction of sudden cardiac death in hypertrophic cardiomyopathyD H Frank Gommans, G Etienne Cramer, Jeannette Bakker, et al.
Human Mutation|May 13, 2008
Genotype-phenotype correlations in MYCN-related Feingold syndromeCarlo L M Marcelis, Frans A Hol, Gail E Graham, et al.
Journal of Pediatric Surgery|December 10, 2013
First results of a European multi-center registry of patients with anorectal malformationsIvo de Blaauw, Charlotte H W Wijers, Eberhard Schmiedeke, et al.
Pageof 4