Neuromotor deficits in children with the 22q11 deletion syndrome. - Wikidata - wikimedia - TriplyDB

Neuromotor deficits in children with the 22q11 deletion syndrome.

Neuromotor deficits in children with the 22q11 deletion syndrome.

http://www.wikidata.org/entity/Q37367125

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Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development Variability in Clinical and Anatomical Manifestation of Velocardiofacial Syndrome Presents Diagnostic and Policy Uncertainty.Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approaches.Prodromal symptoms in adolescents with 22q11.2 deletion syndrome and schizotypal personality disorder.22q11.2 deletion syndrome: are motor deficits more than expected for IQ level?Mapping cortical morphology in youth with velocardiofacial (22q11.2 deletion) syndrome.Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome.22q11.2 deletion syndrome Olfactory disorder in children with 22q11 deletion syndrome.The motor profile of primary school-age children with a 22q11.2 deletion syndrome (22q11.2DS) and an age- and IQ-matched control group.Signs of dysarthria in adults with 22q11.2 deletion syndrome.

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Neuromotor deficits in children with the 22q11 deletion syndrome.

http://www.wikidata.org/entity/Q37367125

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

@tr

scientific article published on December 2006

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Neuromotor deficits in children with the 22q11 deletion syndrome.

@en

Neuromotor deficits in children with the 22q11 deletion syndrome.

@nl

type

label

Neuromotor deficits in children with the 22q11 deletion syndrome.

@en

Neuromotor deficits in children with the 22q11 deletion syndrome.

@nl

prefLabel

Neuromotor deficits in children with the 22q11 deletion syndrome.

@en

Neuromotor deficits in children with the 22q11 deletion syndrome.

@nl

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Movement Disorders

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Neuromotor deficits in children with the 22q11 deletion syndrome.

@en

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Jananne Khuri

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Karen Kiley-Brabeck

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Maria Karayiorgou

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Samantha H Monk

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P2860

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

The Philadelphia story: the 22q11.2 deletion: report on 250 patients

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

Associations between prepulse inhibition and executive visual attention in children with the 22q11 deletion syndrome

Lower prepulse inhibition in children with the 22q11 deletion syndrome.

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.

Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise.

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?

Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2).

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2082-2089

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scholarly article

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10.1002/MDS.21103

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12

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Christina Sobin

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2006-12-01T00:00:00Z

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6803647

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16991148

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2753869

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