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Marieke F van Dooren

Showing results (1-10 of 33) with videos related to

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Current Opinion in Obstetrics & Gynecology|July 18, 2009
Premature ovarian failure and gene polymorphismsMarieke F van Dooren, Aida M Bertoli-Avellab, Rogier A Oldenburg
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 25, 2003
Association of congenital diaphragmatic hernia with limb-reduction defectsMarieke F van Dooren, Alice S Brooks, Dick Tibboel, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 20, 2020
[Direct-to-consumer genetic tests in the consulting room]Elianne M Gerrits, Marieke F van Dooren, Annelien L Bredenoord, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 18, 2004
Postmortem findings and clinicopathological correlation in congenital diaphragmatic herniaMarieke F van Dooren, Natascha N T Goemaere, Annelies de Klein, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 4, 2008
Environmental factors in the etiology of esophageal atresia and congenital diaphragmatic hernia: results of a case-control studyJanine F Felix, Marieke F van Dooren, Merel Klaassens, et al.
European Journal of Medical Genetics|September 16, 2023
Genetic diagnostic yield in an 11-year cohort of craniosynostosis patientsLinda Gaillard, Anne Goverde, Marjolein J A Weerts, et al.
The Journal of Craniofacial Surgery|May 19, 2025
Unveiling the Phenotypic Spectrum of Miller Syndrome: A Systematic ReviewVictor L van Roey, Saranda Ombashi, Idilay Kaymaz, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 11, 2008
Non-VACTERL-type anomalies are frequent in patients with esophageal atresia/tracheo-esophageal fistula and full or partial VACTERL associationElisabeth M de Jong, Janine F Felix, Jacqueline A Deurloo, et al.
International Journal of Pediatric Otorhinolaryngology|December 3, 2021
Mandibular distraction to correct severe non-isolated mandibular hypoplasia: The role of drug-induced sleep endoscopy (DISE) in decision makingPleun P J M van der Plas, Koen F M Joosten, Eppo B Wolvius, et al.
Molecular Cytogenetics|July 15, 2009
Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case reportPaula Jp de Vree, Marleen Eh Simon, Marieke F van Dooren, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Current Opinion in Obstetrics & Gynecology|July 18, 2009
Premature ovarian failure and gene polymorphismsMarieke F van Dooren, Aida M Bertoli-Avellab, Rogier A Oldenburg
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 25, 2003
Association of congenital diaphragmatic hernia with limb-reduction defectsMarieke F van Dooren, Alice S Brooks, Dick Tibboel, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 20, 2020
[Direct-to-consumer genetic tests in the consulting room]Elianne M Gerrits, Marieke F van Dooren, Annelien L Bredenoord, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 18, 2004
Postmortem findings and clinicopathological correlation in congenital diaphragmatic herniaMarieke F van Dooren, Natascha N T Goemaere, Annelies de Klein, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 4, 2008
Environmental factors in the etiology of esophageal atresia and congenital diaphragmatic hernia: results of a case-control studyJanine F Felix, Marieke F van Dooren, Merel Klaassens, et al.
European Journal of Medical Genetics|September 16, 2023
Genetic diagnostic yield in an 11-year cohort of craniosynostosis patientsLinda Gaillard, Anne Goverde, Marjolein J A Weerts, et al.
The Journal of Craniofacial Surgery|May 19, 2025
Unveiling the Phenotypic Spectrum of Miller Syndrome: A Systematic ReviewVictor L van Roey, Saranda Ombashi, Idilay Kaymaz, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 11, 2008
Non-VACTERL-type anomalies are frequent in patients with esophageal atresia/tracheo-esophageal fistula and full or partial VACTERL associationElisabeth M de Jong, Janine F Felix, Jacqueline A Deurloo, et al.
International Journal of Pediatric Otorhinolaryngology|December 3, 2021
Mandibular distraction to correct severe non-isolated mandibular hypoplasia: The role of drug-induced sleep endoscopy (DISE) in decision makingPleun P J M van der Plas, Koen F M Joosten, Eppo B Wolvius, et al.
Molecular Cytogenetics|July 15, 2009
Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case reportPaula Jp de Vree, Marleen Eh Simon, Marieke F van Dooren, et al.
Pageof 4