X-linked dyskeratosis congenita in Malaysia.

doi:10.1002/pbc.21203

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

X-linked dyskeratosis congenita in Malaysia.

Pediatric blood & cancer - 1 Feb 2008

Hamidah Alias, Rashid Radhiyah Abdul, Jamal Rahman, Zhao Meina, Kanegane Hirokazu

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cell Cycle Proteins
Share to Child
Share to Dyskeratosis Congenita
Share to Malaysia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Nuclear Proteins

Source

Open in PubMed

Identifiers

PMID: 17417794
DOI: 10.1002/pbc.21203

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

X-linked dyskeratosis congenita in Malaysia.PMID 17417794Read ↗

Dyskeratosis congenita.Semantic proximity Read ↗

Dyskeratosis CongenitaSemantic proximity Read ↗

Dyskeratosis congenitaSemantic proximity Read ↗

Dyskeratosis congenita: a literature review.Semantic proximity Read ↗

[Dyskeratosis congenita].Semantic proximity Read ↗

The genetics of dyskeratosis congenitaSemantic proximity Read ↗

Dyskeratosis congenita in all its forms.Semantic proximity Read ↗

Dyskeratosis Congenita (DC) Registry: identification of new features of DC.Semantic proximity Read ↗

The diagnosis and treatment of dyskeratosis congenita: a reviewSemantic proximity Read ↗

Expanding the clinical phenotype of autosomal dominant dyskeratosis congenita caused by TERT mutationsSemantic proximity Read ↗

Identification of DKC1 gene mutation in an Indian patient.Semantic proximity Read ↗

Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome)Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.