(Q30467451)

English

Gastrointestinal involvement in a woman with dyskeratosis congenita

scientific article

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scholarly article

1 reference

Europe PubMed Central

21 June 2017

Gastrointestinal involvement in a woman with dyskeratosis congenita (English)

1 reference

Europe PubMed Central

21 June 2017

dyskeratosis congenita

1 reference

based on heuristic

inferred from title

author name string

Brown KE

1

1 reference

Europe PubMed Central

21 June 2017

Kelly TE

2

1 reference

Europe PubMed Central

21 June 2017

Myers BM

3

1 reference

Europe PubMed Central

21 June 2017

publication date

1 January 1993

1 reference

Europe PubMed Central

21 June 2017

Digestive Diseases and Sciences

1 reference

Europe PubMed Central

21 June 2017

38

1 reference

Europe PubMed Central

21 June 2017

1

1 reference

Europe PubMed Central

21 June 2017

181-184

1 reference

Europe PubMed Central

21 June 2017

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DYSKERATOSIS CONGENITA. A CASE WITH NEW FEATURES

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dyskeratosis congenita: two examples of this multisystem disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dyskeratosis congenita: an autosomal dominant disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DYSKERATOSIS CONGENITA AND FAMILIAL PANCYTOPENIA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital anemia in hereditary ectodermal dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormality of platelet size and T-lymphocyte proliferation in an autosomal recessive form of dyskeratosis congenita.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dyskeratosis congenita. Report of a large kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dyskeratosis congenita: relationship to Fanconi's anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dyskeratosis congenita

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Etiologic heterogeneity in dyskeratosis congenita

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the gene for dyskeratosis congenita to Xq28

1 reference

https://pubmed.ncbi.nlm.nih.gov/8420755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01296794

1 reference

Europe PubMed Central

21 June 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

21 June 2017

Springer Nature article ID

10.1007/bf01296794

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