Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys. (Q38910708)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2746616%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

title

Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys (English)

1 reference

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4 October 2019

author name string

L M Curfs

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2746616%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

G Schreppers-Tijdink

2

1 reference

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4 October 2019

A Wiegers

3

1 reference

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4 October 2019

M Borghgraef

4

1 reference

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4 October 2019

J P Fryns

5

1 reference

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4 October 2019

language of work or name

English

0 references

publication date

1 July 1989

1 reference

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Journal of Medical Genetics

4 October 2019

published in

1 reference

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4 October 2019

volume

26

1 reference

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4 October 2019

issue

7

1 reference

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4 October 2019

page(s)

443-446

1 reference

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X-linked mental retardation, macro-orchidism, and the Xq27 fragile site

4 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Fragile X chromosome: clinical and cytogenetic studies on cases from seven families.

9 September 2017

1 reference

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The fragile X syndrome II: preliminary data on growth and development in males

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Fragile X trait in a large kindred: transmission also through normal males

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Fragile-X syndrome: diagnosis and research

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Fragile site X chromosomes and X-linked mental retardation in severely retarded boys in a northern Swedish county. A prevalence study.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

The psychological profile of the fragile X syndrome

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Diagnosis of the fragile X syndrome (Martin-Bell syndrome). Clinical findings in 27 males with the fragile site at Xq28.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Effect of folic acid treatment in the fragile X syndrome.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Cognitive and psychiatric variability in three brothers with fragile X syndrome.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Prevalence of the fragile X syndrome in an institution for the mentally handicapped.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Fragile (X) syndrome: a study of the psychological profile in 23 prepubertal patients

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Fragile X syndrome: a common etiology of mental retardation.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Strengths and weaknesses in the intellectual functioning of males with fragile X syndrome.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Developmental and behavioural disturbances in 13 boys with fragile X syndrome

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

X-linked mental retardation with macro-orchidism and marker X chromosomes

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Fragile (X) X-linked mental retardation I: relationship between age and intelligence and the frequency of expression of fragil (X)(q28).

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Familial X-linked mental retardation syndrome associated with minor congenital anomalies, macro-orchidism, and fragile X-chromosome.

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

The fragile X syndrome. A study of 83 families

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015648

Fragile-X syndrome in Hawaii: a summary of clinical experience

22 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2746616

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Preventive screening for the fragile X syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2746616

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.26.7.443

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2746616%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2746616%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

PubMed publication ID

2746616

1 reference