Brief report: A case of autism with interstitial deletion of chromosome 13. (Q50310950)

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scientific article published in April 2001

Language	Label	Description	Also known as
English	Brief report: A case of autism with interstitial deletion of chromosome 13.	scientific article published in April 2001

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

Brief report: A case of autism with interstitial deletion of chromosome 13. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

0 references

author name string

M M Steele

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

M Al-Adeimi

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

V M Siu

3

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

Y S Fan

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

language of work or name

0 references

publication date

1 April 2001

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

Journal of Autism and Developmental Disorders

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

31

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

231-234

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization and comparison of autistic subgroups: 10 years' experience with autistic children

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

12 December 2020

based on heuristic

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Prevalence of the fragile X anomaly amongst autistic twins and singletons

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

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First report of a Canadian epidemiological study of autistic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

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based on heuristic

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Autism, mental retardation, and chromosomal abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

12 December 2020

based on heuristic

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An autosomal genomic screen for autism. Collaborative linkage study of autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

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based on heuristic

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Chromosomal disorders and autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

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A case-control family history study of autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

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Neuropsychiatric assessment of children with autism: a population-based study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

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Electroretinograms in autism: a pilot study of b-wave amplitudes

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

12 December 2020

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A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Emanuel Miller Memorial Lecture 1998. Autism: two-way interplay between research and clinical work

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

12 December 2020

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Brief report: a case of chromosome 22 alteration associated with autistic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

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A case of autism associated with partial tetrasomy 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/11450821

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1010759401344

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/11450821

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