16 results
Behavioural phenotype of noonan syndrome in adulthood
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- European Psychiatry / Volume 26 / Issue S2 / March 2011
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- 16 April 2020, p. 820
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Clinical phenomena of Charlevoix-Saguenay ataxia in two adult brothers
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- European Psychiatry / Volume 26 / Issue S2 / March 2011
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- 16 April 2020, p. 818
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Fluid intelligence and executive functioning: Partial overlap in patients with psychiatric disorders
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- European Psychiatry / Volume 26 / Issue S2 / March 2011
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- 16 April 2020, p. 1215
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Kleefstra syndrome: neuropsychiatric sequelae
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- European Psychiatry / Volume 26 / Issue S2 / March 2011
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- 16 April 2020, p. 819
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P-700 - Social Cognition and the Behavioural Phenotype of 17q21.31 Microdeletion Syndrome
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- European Psychiatry / Volume 27 / Issue S1 / 2012
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- 15 April 2020, p. 1
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P-701 - Executive Dysfunctions as Part of the Behavioural Phenotype of Aarskog-scott Syndrome
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- European Psychiatry / Volume 27 / Issue S1 / 2012
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- 15 April 2020, p. 1
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W01-03 - Neuropsychological Phenotyping of Genetic Syndromes
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- European Psychiatry / Volume 27 / Issue S1 / 2012
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- 15 April 2020, p. 1
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EPA-0225 – Neuropsychiatric Phenotype of Beta-propeller Protein-associated Neurodegeneration (BPAN)
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- European Psychiatry / Volume 29 / Issue S1 / 2014
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- 15 April 2020, p. 1
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Atypical Antipsychotics and Relapsing Psychoses in 22q11.2 Deletion Syndrome
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- European Psychiatry / Volume 30 / Issue S1 / March 2015
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- 15 April 2020, p. 1
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Phelan-mcdermid Syndrome in an Adult Female with Mild Intellectual Disability
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- European Psychiatry / Volume 30 / Issue S1 / March 2015
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- 15 April 2020, p. 1
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EPA-0226 – Neuropsychological Phenotype of 16p11.2 Microdeletion Syndrome
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- European Psychiatry / Volume 29 / Issue S1 / 2014
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- 15 April 2020, p. 1
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P-711 - Genetic Syndromes and the Autism Spectrum
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- European Psychiatry / Volume 27 / Issue S1 / 2012
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- 15 April 2020, p. 1
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P-713 - A de Novo Microdeletion in Chromosome 8q12.3q13.2: Association With Mild Intellectual Disability and Epilepsy?
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- European Psychiatry / Volume 27 / Issue S1 / 2012
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- 15 April 2020, p. 1
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W01-04 - Psychopathology in Rare Genetic Disorders
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- European Psychiatry / Volume 27 / Issue S1 / 2012
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- 15 April 2020, p. 1
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P-712 - Polg Mutation in a Patient With Recurrent Major Depression, Cardiomyopathy and Ataxia
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- European Psychiatry / Volume 27 / Issue S1 / 2012
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- 15 April 2020, p. 1
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Differentiated psychopharmacological treatment in three genetic subtypes of 22q11.2 deletion syndrome
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- European Psychiatry / Volume 41 / Issue S1 / April 2017
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- 23 March 2020, pp. S388-S389
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