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European Psychiatry : the Journal of the Association of European Psychiatrists|December 21, 2022
Triple X syndrome: Psychiatric disorders and impaired social functioning as a risk factorMaarten Otter, Bea C M Campforts, Constance T R M Stumpel, et al.
American Journal of Medical Genetics. Part A|August 18, 2016
Growth pattern in Kabuki syndrome with a KMT2D mutationDina A Schott, Marinus J Blok, Willem J M Gerver, et al.
Journal of Pediatric Genetics|February 21, 2022
Orthopaedic Aspects of SAMS SyndromeDirk E Schrander, Heleen M Staal, Colin A Johnson, et al.
Nuclear Medicine Communications|August 15, 2018
Evaluation of the most commonly used (semi-)quantitative parameters of 18F-FDG PET/CT to detect malignant transformation of neurofibromas in neurofibromatosis type 1Marloes Brinkman, Sander Jentjens, Kitty Boone, et al.
Hormone Research in Paediatrics|October 4, 2021
Follow-Up Study of Growth Hormone Therapy in Children with Kabuki Syndrome: Two-Year Treatment ResultsLieke van Montfort, Willem Jan M Gerver, Berbel L S Kooger, et al.
Bjpsych Open|February 15, 2021
Social functioning and emotion recognition in adults with triple X syndromeMaarten Otter, Peter M L Crins, Bea C M Campforts, et al.
Journal of Neurodevelopmental Disorders|February 24, 2022
Altered subcortical and cortical brain morphology in adult women with 47,XXX: a 7-Tesla magnetic resonance imaging studyChaira Serrarens, Maarten Otter, Bea C M Campforts, et al.
Sleep & Breathing = Schlaf & Atmung|November 28, 2025
Validation of the Dutch sleep-related breathing disorder scale from the pediatric sleep questionnaire: a diagnostic accuracy study using polysomnographyBibi E Becking, Ronald E G Jonkman, Dominique J P M Stumpel, et al.
European Urology|January 31, 2012
Genome-wide analysis of CpG island methylation in bladder cancer identified TBX2, TBX3, GATA2, and ZIC4 as pTa-specific prognostic markersRaju Kandimalla, Angela A G van Tilborg, Lucie C Kompier, et al.
Fetal and Pediatric Pathology|February 17, 2016
Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash SyndromeLisa Maria Hillen, Erik Jan Kamsteeg, Jeroen Schoots, et al.
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