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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Monique van der Voet

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Human Molecular Genetics|February 8, 2013

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disordersZafar Iqbal, Geert Vandeweyer, Monique van der Voet, et al.

Psychiatric Genetics|November 14, 2015

Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014Monica Aas, Gabriëlla A M Blokland, Samuel J R A Chawner, et al.

Disease Models & Mechanisms|January 10, 2017

A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathyCelia Zazo Seco, Anna Castells-Nobau, Seol-Hee Joo, et al.

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Search research articles

Showing results (21-30 of 23) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 23 results.

Human Molecular Genetics|February 8, 2013

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disordersZafar Iqbal, Geert Vandeweyer, Monique van der Voet, et al.

Psychiatric Genetics|November 14, 2015

Disease Models & Mechanisms|January 10, 2017

A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathyCelia Zazo Seco, Anna Castells-Nobau, Seol-Hee Joo, et al.

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