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Author/Creator Brunner, H.G.

1. De novo WNT5A‐associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. (24th May 2014)

Authors:
Roifman, M.; Marcelis, C.L.M.; Paton, T.; Marshall, C.; Silver, R.; Lohr, J.L.; Yntema, H.G.; Venselaar, H.; Kayserili, H.; van Bon, B.; Seaward, G.; FORGE Canada Consortium; Brunner, H.G.; Chitayat, D.
Journal:
Clinical genetics
Issue:
Volume 87:Number 1(2015:Jan.)
Page Start:
34
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing. (February 2017)

Authors:
Khandelwal, K.D.; Ishorst, N.; Zhou, H.; Ludwig, K.U.; Venselaar, H.; Gilissen, C.; Thonissen, M.; van Rooij, I.A.L.M.; Dreesen, K.; Steehouwer, M.; van de Vorst, M.; Bloemen, M.; van Beusekom, E.; Roosenboom, J.; Borstlap, W.; Admiraal, R.; Dormaar, T.; Schoenaers, J.; Vander Poorten, V.; Hens, G.
Journal:
Journal of dental research
Issue:
Volume 96:Number 2(2017)
Page Start:
179
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗