Showing results (1-10 of 29) with videos related to
Sort By:
Pageof 3
Orphanet Journal of Rare Diseases|July 13, 2006
Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)Griet Van Buggenhout, Jean-Pierre FrynsEuropean Journal of Human Genetics : EJHG|May 21, 2009
Angelman syndrome (AS, MIM 105830)Griet Van Buggenhout, Jean-Pierre FrynsEuropean Journal of Medical Genetics|February 12, 2008
MesiodensGriet Van Buggenhout, Isabelle Bailleul-ForestierMolecular Syndromology|February 6, 2020
Deep Phenotyping of Development, Communication and Behaviour in Phelan-McDermid SyndromeGilles Droogmans, Ann Swillen, Griet Van BuggenhoutEuropean Journal of Medical Genetics|February 16, 2023
Consensus recommendations on altered sensory functioning in Phelan-McDermid syndromeMargreet Walinga, Sarah Jesse, Norma Alhambra, et al.Developmental Medicine and Child Neurology|December 8, 2022
Neurodevelopmental profile and stages of regression in Phelan-McDermid syndromeYumi Dille, Lieven Lagae, Ann Swillen, et al.Journal of Applied Research in Intellectual Disabilities : JARID|February 1, 2021
Stressed parents, happy parents. An assessment of parenting stress and family quality of life in families with a child with Phelan-McDermid syndromeGilles Droogmans, Elfi Vergaelen, Griet Van Buggenhout, et al.Current Opinion in Psychiatry|December 5, 2020
Recent developments in Phelan-McDermid syndrome research: an update on cognitive development, communication and psychiatric disordersAnnick Vogels, Gilles Droogmans, Elfi Vergaelen, et al.Journal of Communication Disorders|March 12, 2004
Speech and language in Wolf-Hirschhorn syndrome: a case-studyJohn Van Borsel, Sigrid De Grande, Griet Van Buggenhout, et al.American Journal of Medical Genetics. Part A|November 4, 2004
A dysmorphic boy with 4qter deletion and 4q32.3-34.3 duplication: clinical, cytogenetic, and molecular findingsGriet Van Buggenhout, Nicole M C Maas, Jean-Pierre Fryns, et al.Pageof 3