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English
Familial X-linked mental retardation with an X chromosome abnormality
scientific article published on February 1, 1977
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
retrieved
28 July 2017
title
Familial X-linked mental retardation with an X chromosome abnormality
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
retrieved
28 July 2017
author name string
J. Harvey
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839500
retrieved
1 August 2022
C. Judge
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839500
retrieved
1 August 2022
S. Wiener
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839500
retrieved
1 August 2022
language of work or name
English
0 references
publication date
1 February 1977
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
retrieved
28 July 2017
full work available at URL
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/839500/?tool=EBI
file format
HTML
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839500
retrieved
1 August 2022
http://jmg.bmjjournals.com/cgi/content/abstract/14/1/46
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839500
retrieved
1 August 2022
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/839500/pdf/?tool=EBI
file format
Portable Document Format
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839500
retrieved
1 August 2022
https://europepmc.org/articles/PMC1013506
file format
HTML
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839500
retrieved
1 August 2022
https://europepmc.org/articles/PMC1013506?pdf=render
file format
Portable Document Format
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839500
retrieved
1 August 2022
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
retrieved
28 July 2017
volume
14
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
retrieved
28 July 2017
page(s)
46-50
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
retrieved
28 July 2017
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
retrieved
28 July 2017
cites work
RECESSIVE GENES IN SEVERE 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=1013506
retrieved
21 June 2018
Familial sex-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=1013506
retrieved
21 June 2018
Recessive sex-linked mental retardation in the absence of other recognizable abnormalities. Report of a family
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=1013506
retrieved
21 June 2018
A marker X chromosome
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=1013506
retrieved
21 June 2018
X-linked Mental Retardation Without Physical Abnormality: Renpenning's 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=1013506
retrieved
21 June 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=1013506
retrieved
21 June 2018
Letter: G-banding with heat treatment
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=1013506
retrieved
21 June 2018
Sex differences in the prevalence of 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=1013506
retrieved
31 October 2018
[New system of chromosome banding: the T bands (author's transl)]
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/839500
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.14.1.46
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
839500
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=839500
retrieved
1 August 2022
PMCID
1013506
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
retrieved
28 July 2017
PubMed ID
839500
1 reference
stated in
Europe PubMed Central
PubMed ID
839500
retrieved
28 July 2017
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