Neuropsychological phenotype of a patient with a de novo 970 kb interstitial deletion in the distal 16p11.2 region

por Egger, Jos I M, Verhoeven, Willem M A, Verbeeck, Wim, de Leeuw, Nicole
Publicado 2014

Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene

por Verhoeven, Willem M A, Egger, Jos I M, Janssen, Paddy K C, van Haeringen, Arie
Publicado 2020

Neurosyphilis Mimicking Autoimmune Encephalitis: A Case Report and Review of the Literature

por Daey Ouwens, Ingrid M., Fiolet, Aernoud T.L., Thijs, Roland D., Koehler, Peter J., Verhoeven, Willem M.A.
Publicado 2020

A Patient with Moderate Intellectual Disability and 49, XXXYY Karyotype

por Verhoeven, Willem M A, Egger, Jos I M, Mergler, Sandra, Meijer, Ton A A, Pfundt, Rolph, Willemsen, Marjolein H
Publicado 2022

A de novo CTNNB1 Novel Splice Variant in an Adult Female with Severe Intellectual Disability

por Verhoeven, Willem M A, Egger, Jos I M, Jongbloed, Rob E, van Putten, Marloes Meijer, de Bruin-van Zandwijk, Marieke, Zwemer, Anne-Suus, Pfundt, Rolph, Willemsen, Marjolein H
Publicado 2020