Marie Pegelow

Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development

Myriam Peyrard‐Janvid, Elizabeth J. Leslie, Youssef A. Kousa et al. · The American Journal of Human Genetics · 2013 · 227 citations · Full text

The prevalence of various dental characteristics in the primary and mixed dentition in patients born with non-syndromic unilateral cleft lip with or without cleft palate

Marie Pegelow, Noha F. Alqadi, Agneta Karsten · European Journal of Orthodontics · 2011 · 69 citations · Full text

Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes

Marie Pegelow, Myriam Peyrard‐Janvid, Marco Zucchelli et al. · European Journal of Orthodontics · 2008 · 54 citations · Full text

Family Members, Genetics, Genetic Epidemiology +21

Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome

Myriam Peyrard‐Janvid, Marie Pegelow, Hannele Koillinen et al. · European Journal of Human Genetics · 2005 · 27 citations · Full text

Irf6 Gene, Van Der Woude, Genetic Disorder +7

Association and Mutation Analyses of the <i>IRF6</i> Gene in Families with Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate

Marie Pegelow, Hannele Koillinen, Måns Magnusson et al. · The Cleft Palate-Craniofacial Journal · 2013 · 25 citations