Deletion of chromosome 2q37 and autism: a distinct subtype? (Q33698973)

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scientific article published in June 1999

Language	Label	Description	Also known as
English	Deletion of chromosome 2q37 and autism: a distinct subtype?	scientific article published in June 1999

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

Europe PubMed Central

Deletion of chromosome 2q37 and autism: a distinct subtype? (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

0 references

author name string

Ghaziuddin M

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Burmeister M

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 June 1999

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Autism and Developmental Disorders

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Europe PubMed Central

PubMed publication ID

28 July 2017

29

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

259-263

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Europe PubMed Central

PubMed publication ID

28 July 2017

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial 6p trisomy associated with infantile autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

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/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization and sequence analysis of the human homeobox-containing gene GBX2

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of deletion 2q35----qter and a peculiar phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion 2q: two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36).

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

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/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 5-HT2B receptor gene maps to 2q36.3-2q37.1

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

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/10425588

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/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical phenotype associated with terminal 2q37 deletion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of autism associated with partial tetrasomy 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/10425588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1023088207468

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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