(Q50344873)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

The prevalence and phenomenology of repetitive behavior in genetic syndromes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Joanna Moss

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

author name string

Kate Arron

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Cheryl Burbidge

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Katy Berg

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

language of work or name

English

0 references

publication date

27 November 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

Journal of Autism and Developmental Disorders

17 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

volume

39

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

page(s)

572-588

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037716%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10803-008-0655-6

17 January 2020

exact match

0 references

cites work

Do autistic children have obsessions and compulsions?

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10803-008-0655-6

Ritual, habit, and perfectionism: the prevalence and development of compulsive-like behavior in normal young children

21 January 2018

1 reference

12 December 2020

An analysis of autism in fifty males with the fragile X syndrome.

1 reference

12 December 2020

Neuropsychology of obsessive-compulsive disorder: a review and treatment implications

1 reference

12 December 2020

NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome

1 reference

12 December 2020

Strengthening behavioral research on genetic mental retardation syndromes

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12 December 2020

Behaviour problems in Angelman syndrome

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12 December 2020

Animal models of restricted repetitive behavior in autism

1 reference

12 December 2020

The influence of visual and ambulation restrictions on stereotyped behavior

1 reference

12 December 2020

Further delineation of the executive deficit in males with fragile-X syndrome.

1 reference

12 December 2020

Cognitive and behavioral profile of the oculocerebrorenal syndrome of Lowe

1 reference

12 December 2020

Angelman syndrome: are the estimates too low?

1 reference

12 December 2020

Brief report: autistic behaviors among children with fragile X or Rett syndrome: implications for the classification of pervasive developmental disorder.

1 reference

12 December 2020

Obsessions and compulsions in Prader-Willi syndrome.

1 reference

12 December 2020

Brief report: cognitive and behavioral profiles in persons with Smith-Magenis syndrome.

1 reference

12 December 2020

Behavioral phenotypes in four mental retardation syndromes: fetal alcohol syndrome, Prader-Willi syndrome, fragile X syndrome, and tuberosis sclerosis

1 reference

12 December 2020

Cognitive and behavioral profile of fragile X boys: correlations to molecular data

1 reference

12 December 2020

Prevalence of maladaptive behavior in retarded children as a function of IQ and age

1 reference

12 December 2020

Evidence for a discrete behavioral phenotype in the oculocerebrorenal syndrome of Lowe.

1 reference

12 December 2020

Maladaptive behaviour in Prader-Willi syndrome in adult life

1 reference

12 December 2020

Advances in research on the fragile X syndrome

1 reference

12 December 2020

The Brachmann-de Lange syndrome

1 reference

12 December 2020

A method of rating behaviour characteristies for use in large scale surveys of mental handicap

1 reference

12 December 2020

A survey of the prevalence of stereotypy, self-injury and aggression in children and young adults with Cri du Chat syndrome

1 reference

12 December 2020

Prevalence study of Prader-Willi syndrome in North Dakota

1 reference

12 December 2020

The Stereotyped Behavior Scale for adolescents and adults with mental retardation.

1 reference

12 December 2020

Advances in autism genetics: on the threshold of a new neurobiology

1 reference

12 December 2020

Stereotyped behaviours in blind children.

1 reference

12 December 2020

Problem behaviors associated with deletion Prader-Willi, Smith-Magenis, and cri du chat syndromes.

1 reference

12 December 2020

Distinctiveness and correlates of maladaptive behaviour in children and adolescents with Smith-Magenis syndrome

1 reference

12 December 2020

Maladaptive behavior in children with Prader-Willi syndrome, Down syndrome, and nonspecific mental retardation

1 reference

12 December 2020

Self-injurious behavior, self-restraint, and compulsive behaviors in Cornelia de Lange syndrome

1 reference

12 December 2020

Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases

1 reference

12 December 2020

Is Angelman syndrome an alternate result of del(15)(q11q13)?

1 reference

12 December 2020

The spasmodic upper-body squeeze: a characteristic behavior in Smith-Magenis syndrome

1 reference

12 December 2020

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

1 reference

12 December 2020

Cognitive functioning in children with typical cri du chat (5p-) syndrome.

1 reference

12 December 2020

Communication, social-emotional development and parenting stress in Cornelia-de-Lange syndrome

1 reference

12 December 2020

Risk markers associated with challenging behaviours in people with intellectual disabilities: a meta-analytic study.

1 reference

12 December 2020

Prader-Willi and Angelman syndromes: sister imprinted disorders

1 reference

12 December 2020

Rituals and compulsivity in Prader-Willi syndrome: profile and stability

1 reference

12 December 2020

Self-injurious behaviour in individuals with intellectual disabilities

1 reference

12 December 2020

Specification of the neurobehavioral phenotype in males with fragile X syndrome.

1 reference

12 December 2020

Autism screening questionnaire: diagnostic validity.

1 reference

12 December 2020

Obsessive-compulsive disorder in mentally retarded patients.

1 reference

12 December 2020

Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation

1 reference

12 December 2020

Measuring behavioral phenotypes: provocations from the "new genetics".

1 reference

12 December 2020

X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations

1 reference

12 December 2020

Developmental and behavioural characteristics of cri du chat syndrome

1 reference

12 December 2020