(Q50310930)

2 March 2018

title

A case report of two male siblings with autism and duplication of Xq13-q21, a region including three genes predisposing for autism. (English)

1 reference

2 March 2018

0 references

1 reference

5

Christopher Gillberg

1 reference

2 March 2018

Elisabet Wentz

1

1 reference

2 March 2018

Mihailo Vujic

series ordinal

2

1 reference

2 March 2018

Ewa-Lotta Kärrstedt

series ordinal

3

1 reference

2 March 2018

Anna Erlandsson

series ordinal

4

1 reference

2 March 2018

publication date

23 August 2013

1 reference

2 March 2018

European Child & Adolescent Psychiatry

published in

1 reference

2 March 2018

volume

23

1 reference

2 March 2018

issue

5

1 reference

2 March 2018

page(s)

329-336

1 reference

2 March 2018

https://scigraph.springernature.com/pub.10.1007/s00787-013-0455-1

exact match

0 references

cites work

A new syndrome with mental retardation, short stature and an Xq duplication.

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

Growth hormone deficiency and empty sella syndrome in a boy with dup(X) (q13.3----q21.2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

Inherited inverted duplication of X chromosome in a male: report of a patient and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

A novel X-linked disorder with developmental delay and autistic features

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

Xq chromosome duplication in males: clinical, cytogenetic and array CGH characterization of a new case and review.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

Behavior checklist for identifying severely handicapped individuals with high levels of autistic behavior.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

Prevalence of autism in an urban population of adults with severe intellectual disabilities--a preliminary study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

X linked mental retardation: a clinical guide

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

A synaptic trek to autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

The HOPA gene dodecamer duplication is not a significant etiological factor in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

Association studies of the HOPA dodecamer duplication variant in different subtypes of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

Transcriptional profiling of fibroblasts from patients with mutations in MCT8 and comparative analysis with the human brain transcriptome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

Craniosynostosis, telecanthus, scalp hair abnormalities, and sensorineural deafness in two sibs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

A case of autism in a child with Apert's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-013-0455-1

Inherited tandem duplication dup(X) (q131-q212) in a male proband

21 January 2018

1 reference

12 December 2020

Inherited tandem duplication of the X chromosome: dup(X)(q13.2-q21.2) in a family.

1 reference

12 December 2020

An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region

1 reference

12 December 2020

Tandem duplication dup(X)(q13q22) in a male proband inherited from the mother showing mosaicism of X-inactivation

1 reference

12 December 2020

Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12-->q13.3) inherited from the mother.

1 reference

12 December 2020

Physical mapping of an Xq-proximal interstitial duplication in a male

1 reference

12 December 2020

Autism spectrum disorders in children with physical or mental disability or both. I: Clinical and epidemiological aspects

1 reference

12 December 2020

Xq13.2q21.1 duplication encompassing the ATRX gene in a man with mental retardation, minor facial and genital anomalies, short stature and broad thorax

1 reference

12 December 2020

10.1007/S00787-013-0455-1

Identifiers

DOI

1 reference

2 March 2018

1 reference

2 March 2018