(Q50306464)

English

Brief report: autism of the Asperger type associated with an autosomal fragile site.

scientific article published in December 1990

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

Brief report: autism of the Asperger type associated with an autosomal fragile site. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

Asperger syndrome

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author name string

J R Saliba

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

M Griffiths

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

language of work or name

0 references

publication date

1 December 1990

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

Journal of Autism and Developmental Disorders

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

20

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

569-575

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic-acid-sensitive fragile sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism is associated with the fragile-X syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile autism: a genetic study of 21 twin pairs

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fra(2) (q13) and inv(9) (p11q12) in autism: causal relationship?

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asperger's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population cytogenetics of autosomal fragile sites.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pervasive developmental disorders and psychoses in adult life.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism, mental retardation, and chromosomal abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome Breakage in Infantile Autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of the fragile X syndrome in infantile autism. A Swedish multicenter study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome abnormalities in infantile autism and other childhood psychoses: a population study of 66 cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A fragile secondary constriction on chromosome 2 in a severely mentally retarded patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asperger's syndrome: a clinical account

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable fragile sites on human chromosomes. XII. Population cytogenetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/2279974

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02216061

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/2279974

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