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English
A new form of X-linked mental retardation with growth retardation, deafness, and microgenitalism.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
title
A new form of X-linked mental retardation with growth retardation, deafness, and microgenitalism
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
main subject
deafness
1 reference
based on heuristic
inferred from title
author name string
R C Juberg
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
I Marsidi
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
language of work or name
English
0 references
publication date
1 September 1980
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
volume
32
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
issue
5
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
page(s)
714-722
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
cites work
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=1686104
retrieved
6 July 2018
An X-linked, recessively inherited syndrome characterized by grave mental deficiency, epilepsy, and endocrine disorder
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=1686104
retrieved
6 July 2018
X-linked mental retardation and-or hydrocephalus
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=1686104
retrieved
6 July 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=1686104
retrieved
6 July 2018
X-linked mental retardation associated with macro-orchidism
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=1686104
retrieved
6 July 2018
Familial X-linked mental retardation with an X chromosome abnormality
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=1686104
retrieved
6 July 2018
X-linked skeletal dysplasia with 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=1686104
retrieved
6 July 2018
More on marker X chromosomes, mental retardation and macro-orchidism
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=1686104
retrieved
6 July 2018
X-linked hypogonadism, gynecomastia, mental retardation, short stature, and obesity--a new 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=1686104
retrieved
6 July 2018
Carrier detection in 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=1686104
retrieved
6 July 2018
Marker X chromosomes, mental retardation and macro-orchidism
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=1686104
retrieved
6 July 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=1686104
retrieved
6 July 2018
Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics
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=1686104
retrieved
6 July 2018
X-linked recessively inherited non-specific mental retardation. Report of a large 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=1686104
retrieved
6 July 2018
Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture
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=1686104
retrieved
6 July 2018
Sex-linked spastic paraplegia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6107045
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1686104
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
PubMed ID
6107045
1 reference
stated in
Europe PubMed Central
PMCID
1686104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6107045%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
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