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S van Dijk

Showing results (81-90 of 119) with videos related to

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European Journal of Human Genetics : EJHG|August 11, 2011
EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfectaFleur S van Dijk, Peter H Byers, Raymond Dalgleish, et al.
Computer Methods in Biomechanics and Biomedical Engineering|April 10, 2019
An interactive surgical simulation tool to assess the consequences of a partial glossectomy on a biomechanical model of the tongueK D R Kappert, M J A van Alphen, S van Dijk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 2, 2020
Prospective clinical investigations of children with periodontal Ehlers-Danlos syndrome identify generalized lack of attached gingiva as a pathognomonic featureInes Kapferer-Seebacher, Elizabeth Oakley-Hannibal, Ulrike Lepperdinger, et al.
European Journal of Medical Genetics|August 14, 2022
Amniotic band sequence in vascular Ehlers-Danlos Syndrome (EDS): Experience of the EDS National Diagnostic Services in the UKSchaida Schirwani, Fleur S van Dijk, Matthew Cauldwell, 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.
Psycho-Oncology|March 4, 2005
Hereditary melanoma and predictive genetic testing: why not?S R Riedijk, F A de Snoo, S van Dijk, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 16, 2010
Lethal/severe osteogenesis imperfecta in a large family: a novel homozygous LEPRE1 mutation and bone histological findingsFleur S van Dijk, Peter G J Nikkels, Nicolette S den Hollander, 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 Human Genetics : EJHG|December 28, 2024
Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhoodNiamh R Wilkinson, Elena Cervi, Bart Wagner, 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.
Pageof 12

Showing results (81-90 of 119) with videos related to

Sort By:
Pageof 12
European Journal of Human Genetics : EJHG|August 11, 2011
EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfectaFleur S van Dijk, Peter H Byers, Raymond Dalgleish, et al.
Computer Methods in Biomechanics and Biomedical Engineering|April 10, 2019
An interactive surgical simulation tool to assess the consequences of a partial glossectomy on a biomechanical model of the tongueK D R Kappert, M J A van Alphen, S van Dijk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 2, 2020
Prospective clinical investigations of children with periodontal Ehlers-Danlos syndrome identify generalized lack of attached gingiva as a pathognomonic featureInes Kapferer-Seebacher, Elizabeth Oakley-Hannibal, Ulrike Lepperdinger, et al.
European Journal of Medical Genetics|August 14, 2022
Amniotic band sequence in vascular Ehlers-Danlos Syndrome (EDS): Experience of the EDS National Diagnostic Services in the UKSchaida Schirwani, Fleur S van Dijk, Matthew Cauldwell, 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.
Psycho-Oncology|March 4, 2005
Hereditary melanoma and predictive genetic testing: why not?S R Riedijk, F A de Snoo, S van Dijk, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 16, 2010
Lethal/severe osteogenesis imperfecta in a large family: a novel homozygous LEPRE1 mutation and bone histological findingsFleur S van Dijk, Peter G J Nikkels, Nicolette S den Hollander, 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 Human Genetics : EJHG|December 28, 2024
Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhoodNiamh R Wilkinson, Elena Cervi, Bart Wagner, 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.
Pageof 12