Marijn A. Creton

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 11 publications

Timeline of Amelogenesis Imperfecta Management.

Timeline of Amelogenesis Imperfecta Management.

Journal: The Journal of craniofacial surgery

Published: February 26, 2025

Is there more to hypodontia then missing teeth?

Is there more to hypodontia then missing teeth?

Journal: Nederlands tijdschrift voor tandheelkunde

Published: June 06, 2023

Concurrent de novo ZFHX4 variant and 16q24.1 deletion in a patient with orofacial clefting; a potential role of ZFHX4 and USP10.

Concurrent de novo ZFHX4 variant and 16q24.1 deletion in a patient with orofacial clefting; a potential role of ZFHX4 and USP10.

Journal: American journal of medical genetics. Part A

Published: August 04, 2022

Gastrointestinal symptoms in patients with isolated oligodontia and a Wnt gene mutation.

Gastrointestinal symptoms in patients with isolated oligodontia and a Wnt gene mutation.

Journal: Oral diseases

Published: September 23, 2020

Oral Health-Related Quality of Life in Dutch Children Diagnosed with Oligodontia. A Cross-Sectional Study.

Oral Health-Related Quality of Life in Dutch Children Diagnosed with Oligodontia. A Cross-Sectional Study.

Journal: International journal of environmental research and public health

Published: June 03, 2019

Concurrent manifestation of oligodontia and thrombocytopenia caused by a contiguous gene deletion in 12p13.2: A three-generation clinical report.

Concurrent manifestation of oligodontia and thrombocytopenia caused by a contiguous gene deletion in 12p13.2: A three-generation clinical report.

Journal: Molecular genetics & genomic medicine

Published: December 20, 2018

Biallelic variants in POLR3GL cause endosteal hyperostosis and oligodontia.

Biallelic variants in POLR3GL cause endosteal hyperostosis and oligodontia.

Journal: European journal of human genetics : EJHG

Published: November 06, 2018

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

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

Journal: European journal of human genetics : EJHG

Published: January 21, 2016

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

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

Journal: European journal of human genetics : EJHG

Published: January 15, 2016

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

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

Journal: American journal of human genetics

Published: June 03, 2015

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

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

Journal: Journal of medical genetics

Published: May 15, 2012

Showing 1-11 of 11

Last Updated: 09/26/2026