Clinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes-Reference-Cited by-同舟云学术

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Clinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes

Published:2020-09-17 Issue:5 Volume:43 Page:e727-e735
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Farah Roula A.,Nair Pratibha,Koueik Jack,Yammine Tony,Khalifeh Hassan,Korban Rima,Collet Agnes,Khayat Claudia,Dubois-Denghien Catherine,Chouery Eliane,Blanluet Maud,El-Hayek Stephany,Stoppa-Lyonnet Dominique,Megarbane Andre

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference25 articles.

1. Fanconi anemia;Soulier;Hematology Am Soc Hematol Educ Program,2011

2. Fanconi anaemia;Tischkowitz;J Med Genet,2003

3. Current diagnosis of inherited bone marrow failure syndromes;Tamary;Pediatr Hematol Oncol,2007

4. Fanconi anaemia and the repair of Watson and Crick DNA crosslinks;Kottemann;Nature,2013

5. The Fanconi anemia pathway and ICL repair: implications for cancer therapy;Wang;Crit Rev Biochem Mol Biol,2010

Cited by 2 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. Longitudinal clinical manifestations of Fanconi anemia: A systematized review;Blood Reviews;2024-08

2. Catalogue for Transmission Genetics in Arabs (CTGA) Database: Analysing Lebanese Data on Genetic Disorders;Genes;2021-09-27

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