(Q50308107)

English

A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autism.

scientific article published in December 1987

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autism. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

0 references

fragile X syndrome

1 reference

based on heuristic

inferred from title

author name string

R Paul

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

E Dykens

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

J F Leckman

3

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

M Watson

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

W R Breg

5

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

D J Cohen

6

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

language of work or name

0 references

publication date

1 December 1987

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

Journal of Autism and Developmental Disorders

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

17

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

457-468

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

https://scigraph.springernature.com/pub.10.1007/bf01486963

0 references

An anthropometric study of males with the fragile-X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked nonspecific mental retardation:Report of a large kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X syndrome: its relations to speech and language disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked recessively inherited non-specific mental retardation. Report of a large family

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further delineation of X-linked mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial sex-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of fragile X syndrome with autism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transmission of fragile (X) (q27) site from a male

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X in a normal male: a cautionary tale

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism and the fragile X syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recessive sex-linked mental retardation in the absence of other recognizable abnormalities. Report of a family

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

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/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial X-linked mental retardation, verbal disability, and marker X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of deinstitutionalization on adaptive behavior of mentally retarded adults

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restudy of the original marker X family

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A marker X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fragile X syndrome. A study of 83 families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X in a survey of 75 autistic males.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile autism associated with the fragile-X syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01486963

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/3479423

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