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Recurrence risks in mental retardation
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Recurrence risks in mental retardation
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
author
Yanick J. Crow
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
author name string
J L Tolmie
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
language of work or name
English
0 references
publication date
1 March 1998
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
volume
35
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
page(s)
177-182
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
cites work
A new strategy for cryptic telomeric translocation screening in patients with idiopathic 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=1051238
retrieved
14 July 2018
Arch fingerprints, hypotonia, and areflexia associated with 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=1051238
retrieved
14 July 2018
Symmetry of neurological signs in Pakistani patients with probable inherited spastic cerebral palsy
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=1051238
retrieved
14 July 2018
The prevalence of mental retardation: a critical review of recent literature.
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=1051238
retrieved
14 July 2018
Fragile X syndrome is less common than previously estimated
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=1051238
retrieved
14 July 2018
XLMR genes: update 1996.
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=1051238
retrieved
14 July 2018
Syndromes with lissencephaly
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=1051238
retrieved
14 July 2018
Mental retardation: genetic findings, clinical implications and research agenda
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=1051238
retrieved
14 July 2018
The detection of subtelomeric chromosomal rearrangements in idiopathic 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=1051238
retrieved
14 July 2018
DNA testing for fragile X syndrome in schools for learning difficulties
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=1051238
retrieved
14 July 2018
Diagnostic yield of the neurologic assessment of the developmentally delayed child
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=1051238
retrieved
14 July 2018
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=1051238
retrieved
14 July 2018
Recurrence risks in severe undiagnosed mental deficiency
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=1051238
retrieved
14 July 2018
A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology
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=1051238
retrieved
14 July 2018
Autosomal recessive or sex linked recessive: a counselling dilemma
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=1051238
retrieved
14 July 2018
The risk of having a second retarded child
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=1051238
retrieved
14 July 2018
Aetiology of mild 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=1051238
retrieved
14 July 2018
Autism and genetics. A decade of research
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=1051238
retrieved
14 July 2018
The recurrence risks for mild idiopathic 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=1051238
retrieved
14 July 2018
Minireview: cryptic translocations and telomere integrity
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=1051238
retrieved
14 July 2018
Colchester revisited: a genetic study of mental defect
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=1051238
retrieved
14 July 2018
Mental retardation and multiple congenital anomalies of unknown etiology: frequency of occurrence in similarly affected sibs of the proband
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=1051238
retrieved
14 July 2018
Diagnostic/genetic studies in severe 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=1051238
retrieved
14 July 2018
Reported biomedical causes and associated medical conditions for mental retardation among 10-year-old children, metropolitan Atlanta, 1985 to 1987.
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=1051238
retrieved
30 October 2018
Mental handicap or learning disability. A critique of political correctness.
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=1051238
retrieved
30 October 2018
Nonspecific X-linked mental retardation II: the frequency in British Columbia.
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=1051238
retrieved
30 October 2018
Sib risks for nonspecific mental retardation in British Columbia.
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=1051238
retrieved
30 October 2018
Prevalence of fragile X syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9541099
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.35.3.177
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
PMC publication ID
1051238
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
PubMed publication ID
9541099
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051238
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9541099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
ResearchGate publication ID
13727821
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