(Q50303895)

2 March 2018

title

A case of autism associated with partial tetrasomy 15 (English)

1 reference

13 June 2024

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7608033

13 June 2024

author name string

M. Hotopf

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7608033

13 June 2024

P. Bolton

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7608033

13 June 2024

language of work or name

English

0 references

publication date

1 February 1995

1 reference

2 March 2018

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF02178166.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF02178166/fulltext.html

13 June 2024

1 reference

http://link.springer.com/content/pdf/10.1007/BF02178166

13 June 2024

1 reference

Journal of Autism and Developmental Disorders

13 June 2024

published in

1 reference

2 March 2018

volume

25

1 reference

2 March 2018

issue

1

1 reference

2 March 2018

page(s)

41-49

1 reference

2 March 2018

An analysis of the parental age effect for inv dup (15).

cites work

1 reference

12 December 2020

Clinical and molecular analysis of five inv dup(15) patients.

1 reference

12 December 2020

Heterogeneity of schizophrenia. Conceptual models and analytic strategies

1 reference

12 December 2020

Autism associated with marker chromosome

1 reference

12 December 2020

Diagnostic assessment in a sample of autistic and developmentally impaired adolescents

1 reference

12 December 2020

Cytogenetic and clinical studies in five cases of inv dup(15)

1 reference

12 December 2020

Hypomelanosis of Ito in Three Cases with Autism and Autistic-like Conditions

1 reference

12 December 2020

Autism and known medical conditions: myth and substance

1 reference

12 December 2020

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome

1 reference

12 December 2020

Partial D 15 trisomy. A case and general review

1 reference

12 December 2020

Prevalence of the fragile X anomaly amongst autistic twins and singletons

1 reference

12 December 2020

The prevalence of fragile X in a sample of autistic individuals diagnosed using a standardized interview.

1 reference

12 December 2020

A case-control family history study of autism

1 reference

12 December 2020

The morbid anatomy of the human genome: chromosomal location of mutations causing disease

1 reference

12 December 2020

Autism diagnostic interview: a standardized investigator-based instrument

1 reference

12 December 2020

Autism as a strongly genetic disorder: evidence from a British twin study

1 reference

12 December 2020

Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome

1 reference

12 December 2020

Partial trisomy of chromosome 15.

1 reference

12 December 2020

Inv dup (15) with mental retardation but few dysmorphic features

1 reference

12 December 2020

Hypomelanosis of ito is frequently associated with autism

series ordinal

27

1 reference

13 June 2024

Identifiers

DOI

10.1007/BF02178166

1 reference

2 March 2018

1 reference

2 March 2018