(Q50301502)

English

Genetic counseling in autism and pervasive developmental disorders.

scientific article published in October 1998

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scholarly article

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/9813780

1 reference

Europe PubMed Central

Genetic counseling in autism and pervasive developmental disorders. (English)

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/9813780

0 references

author name string

E Simonoff

1

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/9813780

language of work or name

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publication date

1 October 1998

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/9813780

Journal of Autism and Developmental Disorders

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/9813780

28

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/9813780

447-456

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/9813780

5

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/9813780

https://scigraph.springernature.com/pub.10.1023/a:1026060623511

0 references

Children with autistic spectrum disorder and a family history of affective disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychiatric family history and neurological disease in autistic spectrum disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Obstetric complications in autism: consequences or causes of the condition?

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mental retardation: genetic findings, clinical implications and research agenda

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

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/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism: the phenotype in relatives.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The UCLA-University of Utah epidemiologic survey of autism: genealogical analysis of familial aggregation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism, affective and other psychiatric disorders: patterns of familial aggregation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

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/9813780

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/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A broader phenotype of autism: the clinical spectrum in twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A family history study of neuropsychiatric disorders in the adult siblings of autistic individuals.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism, affective disorders, and social phobia

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal disorders and autism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

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/9813780

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/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage strategies for genetically complex traits. I. Multilocus models

1 reference

https://pubmed.ncbi.nlm.nih.gov/9813780

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/9813780

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1026060623511

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/9813780

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/9813780

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