Fanconi anemia, dyskeratosis congenita, and WT syndrome-Reference-Cited by-同舟云学术

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Fanconi anemia, dyskeratosis congenita, and WT syndrome

Published:1987 Issue:S3 Volume:28 Page:263-278
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Shahidi Nasrollah T.,Opitz John M.,Bernstein Jay

Publisher

Wiley

Subject

Genetics(clinical)

Reference143 articles.

1. Fanconi’s anemia 2

2. (1983): Long-term outcome in Fanconi's anemia: Description of 26 cases and review of the literature. In (ed): “Chromosome Mutation and Neoplasia” New York: Alan R. Liss, pp 43-62.

3. Squamous Cell Carcinoma of the Vulva and Fanconi Anemia

4. Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens

5. Carcinogen-induced chromosome breakage in Fanconi's anaemia heterozygous cells

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Lateral thinking in syndromic congenital cardiovascular disease;Disease Models & Mechanisms;2023-05-01

2. Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability;Frontiers in Oncology;2022-08-25

3. Ocular manifestations and visual functions in patients with Fanconi anaemia;Acta Ophthalmologica;2013-05-07

4. Dyskeratosis Congenita: A historical perspective;Mechanisms of Ageing and Development;2008-01

5. Dyskeratosis congenita: delay in diagnosis and successful treatment of pancytopenia by bone marrow transplantation;British Journal of Dermatology;1992-09

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