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American Journal of Medical Genetics. Part A|April 10, 2014
Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessmentF S Van Dijk, D O Sillence
European Journal of Medical Genetics|December 21, 2010
Solitary median maxillary central incisor and congenital nasal pyriform aperture stenosis combined with asymmetric crying facies and postaxial lower limb reduction defects: a unique combination of featuresF S Van Dijk, H F van Thuijl, A Wermeskerken, et al.
European Journal of Medical Genetics|November 3, 2009
Classification of Osteogenesis Imperfecta revisitedF S Van Dijk, G Pals, R R Van Rijn, et al.
American Journal of Medical Genetics. Part A|December 6, 2024
The Natural History of Dermatosparaxis Ehlers Danlos Syndrome: An Adult Case SeriesC Angwin, P Byers, E Dulfer, et al.
Molecular Syndromology|May 10, 2012
Osteogenesis Imperfecta: A Review with Clinical ExamplesF S van Dijk, J M Cobben, A Kariminejad, et al.
European Journal of Medical Genetics|December 9, 2008
Compound-heterozygous Marfan syndromeF S Van Dijk, B C Hamel, Y Hilhorst-Hofstee, et al.
The British Journal of Dermatology|May 30, 2019
Electron microscopy in the diagnosis of Ehlers-Danlos syndromes: correlation with clinical and genetic investigationsC Angwin, N Ghali, D Baker, et al.
European Journal of Medical Genetics|October 5, 2014
A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disabilityJ M Cobben, M M Weiss, F S van Dijk, et al.
European Journal of Medical Genetics|November 17, 2011
A novel homozygous 5 bp deletion in FKBP10 causes clinically Bruck syndrome in an Indonesian patientE D Setijowati, F S van Dijk, J M Cobben, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|January 31, 2008
Rendu-Osler-Weber disease: update of medical and dental considerationsE C te Veldhuis, A H te Veldhuis, F S van Dijk, et al.
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