Créton MA - Search Results

1

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

Massink MP, Créton MA, Spanevello F, Fennis WM, Cune MS, Savelberg SM, Nijman IJ, Maurice MM, van den Boogaard MJ, van Haaften G. Massink MP, et al. Among authors: creton ma. Am J Hum Genet. 2015 Oct 1;97(4):621-6. doi: 10.1016/j.ajhg.2015.08.014. Epub 2015 Sep 17. Am J Hum Genet. 2015. PMID: 26387593 Free PMC article.

2

[An enamel disorder in two siblings].

Créton MA, Cune MS. Créton MA, et al. Ned Tijdschr Tandheelkd. 2004 Oct;111(10):400-2. Ned Tijdschr Tandheelkd. 2004. PMID: 15553370 Dutch.

3

Patterns of missing teeth in a population of oligodontia patients.

Créton MA, Cune MS, Verhoeven W, Meijer GJ. Créton MA, et al. Int J Prosthodont. 2007 Jul-Aug;20(4):409-13. Int J Prosthodont. 2007. PMID: 17695874

4

[A description of a population with severe oligodontia].

Créton MA, Cune MS, de Putter C, Verhoeven JW, Meijer GJ. Créton MA, et al. Ned Tijdschr Tandheelkd. 2009 Mar;116(3):119-23. Ned Tijdschr Tandheelkd. 2009. PMID: 19382538 Dutch.

5

Dentofacial characteristics of patients with hypodontia.

Créton M, Cune MS, de Putter C, Ruijter JM, Kuijpers-Jagtman AM. Créton M, et al. Clin Oral Investig. 2010 Aug;14(4):467-77. doi: 10.1007/s00784-009-0308-y. Epub 2009 Jul 10. Clin Oral Investig. 2010. PMID: 19590908

6

Radiographic features of mandibular trabecular bone structure in hypodontia.

Créton M, Geraets W, Verhoeven JW, van der Stelt PF, Verhey H, Cune M. Créton M, et al. Clin Implant Dent Relat Res. 2012 Apr;14(2):241-9. doi: 10.1111/j.1708-8208.2009.00246.x. Epub 2009 Oct 16. Clin Implant Dent Relat Res. 2012. PMID: 19843106

7

Implant treatment in patients with severe hypodontia: a retrospective evaluation.

Créton M, Cune M, Verhoeven W, Muradin M, Wismeijer D, Meijer G. Créton M, et al. J Oral Maxillofac Surg. 2010 Mar;68(3):530-8. doi: 10.1016/j.joms.2009.09.012. J Oral Maxillofac Surg. 2010. PMID: 20171472

8

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

van den Boogaard MJ, Créton M, Bronkhorst Y, van der Hout A, Hennekam E, Lindhout D, Cune M, Ploos van Amstel HK. van den Boogaard MJ, et al. J Med Genet. 2012 May;49(5):327-31. doi: 10.1136/jmedgenet-2012-100750. J Med Genet. 2012. PMID: 22581971 Free article.

9

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

Créton M, van den Boogaard MJ, Maal T, Verhamme L, Fennis W, Carels C, Kuijpers-Jagtman AM, Cune M. Créton M, et al. Clin Oral Investig. 2013 Jun;17(5):1437-45. doi: 10.1007/s00784-012-0828-8. Epub 2012 Aug 31. Clin Oral Investig. 2013. PMID: 22936299

10

Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome).

Monroe GR, Kappen IF, Stokman MF, Terhal PA, van den Boogaard MH, Savelberg SM, van der Veken LT, van Es RJ, Lens SM, Hengeveld RC, Creton MA, Janssen NG, Mink van der Molen AB, Ebbeling MB, Giles RH, Knoers NV, van Haaften G. Monroe GR, et al. Among authors: creton ma. Eur J Hum Genet. 2016 Dec;24(12):1752-1760. doi: 10.1038/ejhg.2016.103. Epub 2016 Aug 17. Eur J Hum Genet. 2016. PMID: 27530628 Free PMC article.

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