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English
A postulated mechanism for deletions with inversions
scientific article published in May 1993
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
title
A postulated mechanism for deletions with inversions
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
author name string
Sommer SS
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
Ketterling RP
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
language of work or name
English
0 references
publication date
1 May 1993
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
volume
52
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
page(s)
1016-1018
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
issue
5
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
cites work
Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patients.
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=1682059
retrieved
25 May 2018
Nucleotide sequence of the gene for human factor IX (antihemophilic factor B)
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=1682059
retrieved
25 May 2018
Recombination between two 14-bp homologous sequences as the mechanism for gene deletion in factor IX Seattle 1.
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=1682059
retrieved
25 May 2018
Somatic mosaicism in a patient with bilateral retinoblastoma
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=1682059
retrieved
25 May 2018
Factor IXMadrid 2: a deletion/insertion in factor IX gene which abolishes the sequence of the donor junction at the exon IV-intron d splice site
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=1682059
retrieved
25 May 2018
Parental origin of factor IX gene mutations, and their distribution in the 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=1682059
retrieved
25 May 2018
Identifiers
PMCID
1682059
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
PubMed ID
8488833
1 reference
stated in
Europe PubMed Central
PMCID
1682059
retrieved
14 November 2017
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