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American Journal of Medical Genetics. Part A|May 15, 2024
Neuropsychological functioning of adults with PTEN hamartoma tumor syndromeCarmen Oldenboom, Meggie M C M Drissen, Linde C M van Dongen, et al.
Genes, Brain, and Behavior|July 9, 2021
Speech-language profiles in the context of cognitive and adaptive functioning in SATB2-associated syndromeLot Snijders Blok, Y Max Goosen, Leenke van Haaften, et al.
Psychopathology|March 24, 2012
Cerebellar cognitive affective syndrome and autosomal recessive spastic ataxia of charlevoix-saguenay: a report of two male sibsWillem M A Verhoeven, Jos I M Egger, Amir I M Ahmed, et al.
Journal of Clinical Medicine|August 26, 2022
Cognitive Phenotype and Psychopathology in Noonan Syndrome Spectrum Disorders through Various Ras/MAPK Pathway Associated Gene VariantsEllen Wingbermühle, Renée L Roelofs, Wouter Oomens, et al.
Parkinsonism & Related Disorders|December 26, 2013
Beta-propeller protein-associated neurodegeneration (BPAN), a rare form of NBIA: novel mutations and neuropsychiatric phenotype in three adult patientsWillem M A Verhoeven, Jos I M Egger, David A Koolen, et al.
American Journal of Medical Genetics. Part A|August 13, 2020
Behavior and cognitive functioning in Witteveen-Kolk syndromeLinde C M van Dongen, Ellen Wingbermühle, Alexander J M Dingemans, et al.
Clinical Neuropsychiatry|December 13, 2023
Measuring Adaptive Behavior in Patients with Mendelian Neurodevelopmental Disorders. Comparison of ABAS-3 and Dutch Vineland ScalesJoost Kummeling, Karlijn Vermeulen-Kalk, Veerle Souverein, et al.
Genes, Brain, and Behavior|February 21, 2019
Exploring the behavioral and cognitive phenotype of KBG syndromeLinde C M van Dongen, Ellen Wingbermühle, William M van der Veld, et al.
American Journal of Medical Genetics. Part A|November 22, 2012
Hypersociability in the behavioral phenotype of 17q21.31 microdeletion syndromeJos I M Egger, Ellen Wingbermühle, Willem M A Verhoeven, et al.
International Medical Case Reports Journal|October 29, 2020
A de novo <i>CTNNB1</i> Novel Splice Variant in an Adult Female with Severe Intellectual DisabilityWillem M A Verhoeven, Jos I M Egger, Rob E Jongbloed, et al.
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