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Partial monosomy of chromosome 10 short arms.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
title
Partial monosomy of chromosome 10 short arms
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
author name string
A Gencík
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
U Brönniman
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
R Tobler
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
P Auf der Maur
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
language of work or name
English
0 references
publication date
1 April 1983
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
volume
20
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
page(s)
107-111
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
cites work
Ring chromosome 10:46,XX,r(10)(p15 leads to q26)
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=1049010
retrieved
27 May 2018
Del(10)p autosomal deletion syndrome: Clinical, cytogenetic and gene marker studies
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=1049010
retrieved
27 May 2018
Physical retardation is associated with ring chromosome mosaicism: 46, XX,r(10)/45, XX,10 minus
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=1049010
retrieved
27 May 2018
10p- syndrome associated with multiple chromosomal abnormalities
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=1049010
retrieved
27 May 2018
Ring 10 chromosome: 46,XX,r10(p15q26).
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=1049010
retrieved
27 May 2018
Partial trisomy 10p in two generations
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=1049010
retrieved
27 May 2018
Ring chromosome 10 Associated with multiple congenital malformations
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=1049010
retrieved
27 May 2018
Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12).
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=1049010
retrieved
27 May 2018
Report of the committee on the genetic constitution of chromosomes 10, 11, 12, X, and Y.
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=1049010
retrieved
27 May 2018
Deletion of the short arm of chromosome No. 10.
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=1049010
retrieved
27 May 2018
Partial monosomy 10p 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=1049010
retrieved
16 August 2018
C-group chromosome abnormality (? 10p-). Occurrence in a child with multiple malformations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6842544
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Deletion of the short arm of chromosome No. 10
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6842544
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Risk for short arm 10 trisomy. A segregation analysis of eleven families with different translocations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6842544
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6842544
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Distal 10p deletion syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6842544
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.20.2.107
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
PMCID
1049010
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
PubMed ID
6842544
1 reference
stated in
Europe PubMed Central
PMCID
1049010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6842544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
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