Publications by authors named "Marie-Jose van den Boogaard"

32Publications

The ontogeny of Robin sequence.

Am J Med Genet A 2018 06 25;176(6):1349-1368. Epub 2018 Apr 25.

Royal Children's Hospital, Murdoch Children's Research Institute, Parkville, Australia.

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http://dx.doi.org/10.1002/ajmg.a.38718DOI Listing
June 2018

Mortality in Robin sequence: identification of risk factors.

Eur J Pediatr 2018 05 28;177(5):781-789. Epub 2018 Feb 28.

Department of Plastic and Reconstructive Surgery, University Medical Centre Utrecht, Wilhelmina Children's Hospital, Utrecht, The Netherlands.

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http://dx.doi.org/10.1007/s00431-018-3111-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899115PMC
May 2018

Robin Sequence: Continuing Heterogeneity in Nomenclature and Diagnosis.

J Craniofac Surg 2018 Jun;29(4):985-987

Division of Plastic and Reconstructive Surgery.

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http://dx.doi.org/10.1097/SCS.0000000000004361DOI Listing
June 2018

Polyhydramnios in isolated oral cleft pregnancies: incidence and outcome in a retrospective study.

Prenat Diagn 2017 Feb 24;37(2):162-167. Epub 2017 Jan 24.

Department of Obstetrics and Gynecology, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1002/pd.4983DOI Listing
February 2017

The association between WNT10A variants and dental development in patients with isolated oligodontia.

Eur J Hum Genet 2016 01 21;25(1):59-65. Epub 2016 Sep 21.

Department of Oral & Maxillofacial Surgery, Special Dental Care and Orthodontics, Erasmus University Medical Centre, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1038/ejhg.2016.117DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5159758PMC
January 2016

Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia.

Am J Hum Genet 2015 Oct 17;97(4):621-6. Epub 2015 Sep 17.

Department of Medical Genetics, Centre for Molecular Medicine, University Medical Centre Utrecht, 3508 AB Utrecht, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.08.014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596913PMC
October 2015

Etiology and pathogenesis of robin sequence in a large Dutch cohort.

Am J Med Genet A 2015 Sep 31;167A(9):1983-92. Epub 2015 May 31.

Department of Pediatrics, Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands.

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http://dx.doi.org/10.1002/ajmg.a.37154DOI Listing
September 2015

Birth prevalence of Robin sequence in the Netherlands from 2000-2010: a retrospective population-based study in a large Dutch cohort and review of the literature.

Am J Med Genet A 2015 Sep 21;167A(9):1972-82. Epub 2015 May 21.

Department of Plastic, Reconstructive and Hand Surgery, Wilhelmina Children's Hospital, Utrecht, The Netherlands.

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http://dx.doi.org/10.1002/ajmg.a.37150DOI Listing
September 2015

Elevated Infant Mortality Rate among Dutch Oral Cleft Cases: A Retrospective Analysis from 1997 to 2011.

Front Surg 2014 4;1:48. Epub 2014 Dec 4.

Division of Plastic and Reconstructive Surgery, University Medical Center Utrecht , Utrecht , Netherlands.

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http://dx.doi.org/10.3389/fsurg.2014.00048DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286963PMC
January 2015

Reaction to: Persson et al. Educational achievements in Pierre Robin sequence. J Plast Surg Hand Surg 2013;47(1):36-9.

J Plast Surg Hand Surg 2014 Aug 9;48(4):287-8. Epub 2014 Jun 9.

Division of Plastic and Reconstructive Surgery, University of Utrecht Medical Center , Utrecht , The Netherlands.

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http://dx.doi.org/10.3109/2000656X.2014.924956DOI Listing
August 2014

Microtia in the Netherlands: clinical characteristics and associated anomalies.

Int J Pediatr Otorhinolaryngol 2014 Jun 30;78(6):954-9. Epub 2014 Mar 30.

Division of Plastic and Reconstructive Surgery; University of Utrecht Medical Center, Heidelberglaan 100, PO Box 85500, 3508 GA Utrecht, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.ijporl.2014.03.024DOI Listing
June 2014

Three-dimensional analysis of tooth dimensions in the MSX1-missense mutation.

Clin Oral Investig 2013 Jun 31;17(5):1437-45. Epub 2012 Aug 31.

Department of Oral and Maxillofacial Surgery, Prosthodontics and Special Dental Care, University Medical Centre Utrecht, Utrecht, The Netherlands.

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http://link.springer.com/10.1007/s00784-012-0828-8
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http://dx.doi.org/10.1007/s00784-012-0828-8DOI Listing
June 2013

A systematic review of associated structural and chromosomal defects in oral clefts: when is prenatal genetic analysis indicated?

J Med Genet 2012 Aug;49(8):490-8

Department of Plastic and Reconstructive Surgery, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1136/jmedgenet-2012-101013DOI Listing
August 2012

Mutations in WNT10A are present in more than half of isolated hypodontia cases.

J Med Genet 2012 May;49(5):327-31

Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1136/jmedgenet-2012-100750DOI Listing
May 2012

Ectrodactyly with fibular aplasia: a separate entity?

Eur J Med Genet 2008 Sep-Oct;51(5):488-96. Epub 2008 May 2.

Department of Paediatric Genetics, Emma Children's Hospital/Academic Medical Centre, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.

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http://dx.doi.org/10.1016/j.ejmg.2008.04.001DOI Listing
November 2008