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The fragile X syndrome in a large family. II. Psychological investigations
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
title
The fragile X syndrome in a large family. II. Psychological investigations
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
main subject
fragile X syndrome
1 reference
based on heuristic
inferred from title
author name string
H Veenema
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
T Veenema
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
J P Geraedts
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
language of work or name
English
0 references
publication date
1 January 1987
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
volume
24
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
page(s)
32-38
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
cites work
Nonspecific X-linked mental retardation I: a review with information from 24 new families
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
21 June 2018
Nonspecific X-linked mental retardation--a review
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
21 June 2018
The psychological profile of the fragile X syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
21 June 2018
Conference report: International Workshop on the fragile X and X-linked mental retardation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
21 June 2018
Theory of X-linkage of major intellectual traits.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
21 June 2018
X-linked mental retardation without physical abnormality (Renpenning's syndrome) in sibs in an institution.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
21 June 2018
The fragile X syndrome in a large family. I. Cytogenetic and clinical investigations.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
21 June 2018
X-linked nonspecific mental retardation:Report of a large kindred
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
21 June 2018
Familial X-linked mental retardation, verbal disability, and marker X chromosomes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
21 June 2018
X-linked mental retardation: a study of 7 families.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
30 October 2018
X-linked mental retardation and fragile-X or marker-X syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
30 October 2018
Fragile (X) X-linked mental retardation I: relationship between age and intelligence and the frequency of expression of fragil (X)(q28).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
30 October 2018
Marker X-associated mental retardation. A study of 150 retarded males.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
30 October 2018
The fragile X syndrome. A study of 83 families.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049853
retrieved
30 October 2018
Identifiers
DOI
10.1136/JMG.24.1.32
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
PMCID
1049853
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
PubMed ID
3806640
1 reference
stated in
Europe PubMed Central
PMCID
1049853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3806640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 October 2019
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