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DNA repair disorders
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
DNA repair disorders
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
author name string
Woods CG
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
language of work or name
English
0 references
publication date
1 February 1998
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
published in
Archives of Disease in Childhood
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
volume
78
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
page(s)
178-184
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
cites work
Congenital telangiectatic erythema resembling lupus erythematosus in dwarfs; probably a syndrome entity.
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=1717464
retrieved
12 July 2018
Fanconi anaemia forges a novel pathway.
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=1717464
retrieved
12 July 2018
Molecular genetics of Bloom's 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=1717464
retrieved
12 July 2018
Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review
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=1717464
retrieved
12 July 2018
A single ataxia telangiectasia gene with a product similar to PI-3 kinase
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=1717464
retrieved
12 July 2018
Defective Repair Replication of DNA in Xeroderma Pigmentosum
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=1717464
retrieved
12 July 2018
Rate of depurination of native deoxyribonucleic acid
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=1717464
retrieved
12 July 2018
Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 830 published cases
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=1717464
retrieved
12 July 2018
Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.
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=1717464
retrieved
12 July 2018
Cloning of cDNAs for Fanconi's anaemia by functional complementation
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=1717464
retrieved
12 July 2018
Cockayne syndrome: Review of 140 cases
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=1717464
retrieved
12 July 2018
Ataxia-telangiectasia: some historic, clinical and pathologic observations
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=1717464
retrieved
12 July 2018
Different forms of TFIIH for transcription and DNA repair: holo-TFIIH and a nucleotide excision repairosome
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=1717464
retrieved
26 September 2018
Ataxia telangiectasia in the British Isles: the clinical and laboratory features of 70 affected individuals
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9579166
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/ADC.78.2.178
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
PMCID
1717464
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
PubMed ID
9579166
1 reference
stated in
Europe PubMed Central
PubMed ID
9579166
retrieved
7 August 2017
ResearchGate publication ID
270744567
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