(Q50303895)

English

A case of autism associated with partial tetrasomy 15.

scientific article published in February 1995

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

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

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

0 references

author name string

M Hotopf

1

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

P Bolton

2

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

language of work or name

0 references

publication date

1 February 1995

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

Journal of Autism and Developmental Disorders

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

25

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

41-49

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

1

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

https://scigraph.springernature.com/pub.10.1007/bf02178166

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneity of schizophrenia. Conceptual models and analytic strategies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism associated with marker chromosome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic assessment in a sample of autistic and developmentally impaired adolescents

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism and known medical conditions: myth and substance

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial D 15 trisomy. A case and general review

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of the fragile X anomaly amongst autistic twins and singletons.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case-control family history study of autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism diagnostic interview: a standardized investigator-based instrument.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy of chromosome 15.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7608033

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02178166

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/7608033

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