(Q33586647)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:768476%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

review article

1 reference

title

Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:768476%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

main subject

dyskeratosis congenita

1 reference

C. Sirinavin

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A768476

27 July 2022

A. A. Trowbridge

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A768476

27 July 2022

language of work or name

English

0 references

publication date

1 December 1975

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:768476%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

13 September 2019

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/768476/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A768476

http://jmg.bmjjournals.com/cgi/content/abstract/12/4/339

27 July 2022

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A768476

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/768476/pdf/?tool=EBI

27 July 2022

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A768476

https://europepmc.org/articles/PMC1013312

27 July 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A768476

https://europepmc.org/articles/PMC1013312?pdf=render

27 July 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A768476

Journal of Medical Genetics

27 July 2022

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:768476%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

volume

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:768476%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:768476%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

page(s)

339-354

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:768476%20AND%20SRC:MED&resulttype=core&format=json

Dyskeratosis congenita with pigmentation, dystrophia unguium, and leucokeratosis oris; review of the known cases reported to date and discussion of the disease from various aspects

13 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

DYSKERATOSIS CONGENITA. FIRST REPORT OF ITS OCCURRENCE IN A FEMALE AND A REVIEW OF THE LITERATURE.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Congenital dyskeratosis, type Zinsser-Cole-Engman, associated with a constitutional myelopathy (thrombopenic purpura & neutropenia)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Dyskeratosis congenita; relationship to poikiloderma atrophicans vasculare and to aplastic anemia of Fanconi

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Poikiloderma, parapsoriasis and atrophia cutis cum pigmentatione, dystrophia ungium et leukoplakia oris Zinsser, so-called dyskeratosis congenita

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Bone marrow origin of immunologically competent lymphocytes in the rat

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Squamous Cell Carcinomas in Fanconi's Anemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Occurrence of malignancy in immunodeficiency diseases. A literature review

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Xeroderma pigmentosum. An inherited diseases with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Zinsser-Cole-Engman syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Relations between Immunity and Malignancy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Viral infections in man associated with acquired immunological deficiency states.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Hepatoma and peliosis hepatis developing in a patient with Fanconi's anemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Leukemia in Fanconi's anemia: cytogenetic and tumor virus susceptibility studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Chromosomal abnormalities in human neoplasia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Dyskeratosis congenita with pancytopenia. Another constitutional anemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013312

Morphogenetic interactions in the development of the mouse thymus gland

31 October 2018

1 reference

12 December 2020

Congenital anemia in hereditary ectodermal dysplasia

1 reference

12 December 2020

Dyskeratosis congenita

1 reference

12 December 2020

THE ASSOCIATION OF DYSKERATOSIS CONGENITA AND FANCONI'S ANAEMIA

1 reference

12 December 2020

DYSKERATOSIS CONGENITA AND FAMILIAL PANCYTOPENIA

1 reference

12 December 2020

Zinsser-Cole-Engmann congenital dyskeratosis

1 reference

12 December 2020

Congenital dyskeratosis. Zinsser-Engman-Cole syndrome with thymic dysplasia and aplastic anemia

1 reference

12 December 2020

Congenital dyskeratosis with thrombopenia. Its relations with Fanconi's anemia

1 reference

12 December 2020

Zinsser-Engman-Cole syndrome with an extensive dyschromia of the skin

1 reference

12 December 2020

Zinsser-Cole-Engman (Zinsser-Fanconi) syndrome

1 reference

12 December 2020

Leukoplakia, pigment changes and ungual dystrophy. Zinsser-Cole-Engman syndrome--so-called congenital dyskeratosis

1 reference

12 December 2020

[Zinsser-Fanconi syndrome]

1 reference

12 December 2020

On a case of Zinsser-Engman-Cole syndrome

1 reference

12 December 2020

Dyskeratosis congenita

1 reference

12 December 2020

ATAXIA-TELANGIECTASIA. ITS ASSOCIATION WITH A DEFECTIVE THYMUS, IMMUNOLOGICAL-DEFICIENCY DISEASE, AND MALIGNANCY

1 reference

12 December 2020

DYSKERATOSIS CONGENITA. A CASE WITH NEW FEATURES

1 reference

12 December 2020

FANCONI'S ANAEMIA AND DYSKERATOSIS CONGENITA AS A SYNDROME

1 reference

12 December 2020

Dyskeratosis congenita with pigmentation, dystrophia unguium, and leukoplakia oris; a follow-up report of two brothers

1 reference

12 December 2020

[Pathology of dyskeratosis congenita Cole-Rauschkolb-Toomay]

1 reference

12 December 2020

[Congenital dyskeratosis with atresia of the lacrimal points: Zinsser-Engman-Cole disease]

1 reference

12 December 2020

Two Japanese cases of a peculiar reticulous pigmentation

1 reference

12 December 2020

Familial pigmentation with dystrophy of the nails; report of three cases

1 reference

12 December 2020

The so-called "dyskeratosis congenita"; cole, rauschkolb and toomey; pigmentatio parvo-reticularis cum leucoplakia et dystrophia unguium

1 reference

12 December 2020

Dyskeratosis congenita: relationship to Fanconi's anemia

1 reference

12 December 2020

Pneumocystis carinii pneumonia in the United States. Epidemiologic, diagnostic, and clinical features

1 reference

12 December 2020

DNA polymerases I and II in regenerating rat liver and Morris hepatomas

1 reference

12 December 2020

Immunodeficiency disease and malignancy. Various immunologic deficiencies of man and the role of immune processes in the control of malignant disease

1 reference

12 December 2020

Dyskeratosis congenita: two extremes

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.12.4.339

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:768476%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:768476%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

1 reference