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A de novo X;13 translocation with abnormal phenotype
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
title
A de novo X;13 translocation with abnormal phenotype
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
author name string
Hodgson SV
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
Barber JC
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
Dowie A
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
Dubowitz V
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
language of work or name
English
0 references
publication date
1 October 1986
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
volume
23
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
page(s)
477-478
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
cites work
X long-arm deletions. A review of non-mosaic cases studied with banding techniques
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=1049790
retrieved
21 June 2018
Balanced structural changes involving the human X: Effect on sexual phenotype
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=1049790
retrieved
21 June 2018
Two cases of X/autosome translocation in females with incontinentia pigmenti.
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=1049790
retrieved
21 June 2018
Prometaphase banding of human chromosomes with basic fuchsin.
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=1049790
retrieved
30 October 2018
Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3783628
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1049790
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
PubMed ID
3783628
1 reference
stated in
Europe PubMed Central
PubMed ID
3783628
retrieved
28 July 2017
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