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Genetic heterogeneity in multiple epiphyseal dysplasia
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
title
Genetic heterogeneity in multiple epiphyseal dysplasia
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
main subject
heterogeneity
1 reference
based on heuristic
inferred from title
multiple epiphyseal dysplasia
1 reference
based on heuristic
inferred from title
author name string
Deere M
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
Blanton SH
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
Scott CI
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
Langer LO
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
Pauli RM
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
Hecht JT
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
language of work or name
English
0 references
publication date
1 March 1995
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
volume
56
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
page(s)
698-704
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
cites work
Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19
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=1801152
retrieved
20 June 2018
Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19.
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=1801152
retrieved
20 June 2018
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen gene
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=1801152
retrieved
20 June 2018
Strategies for multilocus linkage analysis in humans
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=1801152
retrieved
20 June 2018
Inheritance of multiple epiphyseal dysplasia, tarda
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=1801152
retrieved
20 June 2018
Multiple epiphyseal dysplasia tarda. A family with autosomal recessive inheritance.
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=1801152
retrieved
20 June 2018
Gonadal mosaicism in pseudoachondroplasia.
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=1801152
retrieved
20 June 2018
Exclusion of type II and type VI procollagen gene mutations in a five-generation family with multiple epiphyseal dysplasia.
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=1801152
retrieved
26 November 2018
Hereditary dysplasia epiphysealis multiplex
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7887425
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Multiple epiphyseal dysplasia in two siblings. Histological and biochemical analyses of epiphyseal plate cartilage in one
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7887425
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Linkage of typical pseudoachondroplasia to chromosome 19
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7887425
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1801152
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
PubMed ID
7887425
1 reference
stated in
Europe PubMed Central
PMCID
1801152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7887425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
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