(Q33677997)

English

Rothmund-Thomson syndrome: two case reports show heterogeneous cutaneous abnormalities, an association with genetically programmed ageing changes, and increased chromosomal radiosensitivity

scientific article

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Rothmund-Thomson syndrome: two case reports show heterogeneous cutaneous abnormalities, an association with genetically programmed ageing changes, and increased chromosomal radiosensitivity (English)

1 reference

Europe PubMed Central

28 July 2017

Rothmund-Thomson syndrome

1 reference

based on heuristic

inferred from title

author name string

B Kerr

1

1 reference

Europe PubMed Central

28 July 2017

G S Ashcroft

2

1 reference

Europe PubMed Central

28 July 2017

D Scott

3

1 reference

Europe PubMed Central

28 July 2017

M A Horan

4

1 reference

Europe PubMed Central

28 July 2017

M W Ferguson

5

1 reference

Europe PubMed Central

28 July 2017

D Donnai

6

1 reference

Europe PubMed Central

28 July 2017

language of work or name

0 references

publication date

1 November 1996

1 reference

Europe PubMed Central

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

28 July 2017

33

1 reference

Europe PubMed Central

28 July 2017

11

1 reference

Europe PubMed Central

28 July 2017

928-934

1 reference

Europe PubMed Central

28 July 2017

Instability of lymphocyte chromosomes in a girl with Rothmund-Thomson syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

The effects of ageing on cutaneous wound healing in mammals.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Enhanced radiosensitivity and defective DNA repair in cultured fibroblasts derived from Rothmund Thomson syndrome patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Cell death, chromosome damage and mitotic delay in normal human, ataxia telangiectasia and retinoblastoma fibroblasts after x-irradiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Chromatid damage after G2 phase x-irradiation of cells from cancer-prone individuals implicates deficiency in DNA repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Rothmund-Thomson syndrome. A case report, phototesting, and literature review.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Structural and functional changes of normal aging skin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Chromosome instability syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Skin aging and photoaging: an overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Rothmund-Thomson syndrome associated with trisomy 8 mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Carrier detection in xeroderma pigmentosum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Clonal lines of aneuploid cells in Rothmund-Thomson syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Rothmund-Thomson syndrome: a report of two patients and a review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Rothmund-Thomson syndrome: review of the world literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

G2 chromosomal radiosensitivity in Fanconi's anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

21 June 2018

Rothmund-Thomson syndrome: a case report.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

30 October 2018

Enhanced chromatid damage in blood lymphocytes after G2 phase x irradiation, a marker of the ataxia-telangiectasia gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050787

30 October 2018

Rothmund-Thomson syndrome: an oculocutaneous disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rothmund's syndrome; Thomson's syndrome; congenital poikiloderma with or without juvenile cataracts

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rothmund-Thomson Syndrome With Severe Dwarfism

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of X-irradiation in G1 and G2 on Bloom's Syndrome and normal chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-dermatological complications and genetic aspects of the Rothmund-Thomson syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth hormone deficiency in the Rothmund-Thomson syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factors affecting and significance of G2 chromatin radiosensitivity in predisposition to cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of Rothmund-Thomson syndrome with reduced DNA repair capacity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rothmund-Thomson syndrome associated with annular pancreas and duodenal stenosis: a case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic response to G2-phase X irradiation in relation to DNA repair and radiosensitivity in a cancer-prone family with Li-Fraumeni syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic predisposition in breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro chromosomal radiosensitivity in "chromosomal breakage syndromes"

1 reference

https://pubmed.ncbi.nlm.nih.gov/8950673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.33.11.928

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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0 references

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