The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature-Reference-Cited by-同舟云学术

The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature

Published:2021-05-07 Issue:7 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Thompson Ashley S.¹,Saba Nusrat²,McReynolds Lisa J.¹,Munir Saeeda²,Ahmed Parvez³,Sajjad Sumaira²,Jones Kristine⁴,Yeager Meredith⁴,Donovan Frank X.⁵,Chandrasekharappa Settara C.⁵,Alter Blanche P.¹,Savage Sharon A.¹^ORCID,Rehman Sadia²

Affiliation:

1. Clinical Genetics Branch Division of Cancer Epidemiology and Genetics National Cancer Institute Bethesda MD USA

2. Institute of Biomedical and Genetic Engineering Islamabad Pakistan

3. Quaid‐i‐Azam International Hospital Islamabad Pakistan

4. Cancer Genomics Research Laboratory Leidos Biomedical Research Frederick National Laboratory for Cancer Research Frederick MD 20850 USA

5. Cancer Genetics and Comparative Genomics Branch National Human Genome Research InstituteNational Institutes of Health Bethesda MD USA

Funder

National Human Genome Research Institute

National Cancer Institute

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1693

Reference68 articles.

1. Analysis of FANCC gene mutations (IVS4+4A>T, del322G, and R548X)in patients with Fanconi anemia in Pakistan

2. Thinking of VACTERL-H? Rule out Fanconi Anemia according to PHENOS

3. Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up

4. VACTERL‐H association and fanconi anemia;Alter B. P.;Molecular Syndromology,2013

5. Diagnosis of Fanconi Anemia: Mutation Analysis by Next-Generation Sequencing

Cited by 3 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. An acquired BMF with FANCL gene heterozygous mutation: Case report;Medicine;2023-06-16

2. Inherited bone marrow failure syndromes: a review of current practices and potential future research directions;Current Opinion in Pediatrics;2022-11-10

3. Frequency Determination of c.1115_1118delTTGG and c.3788_3790delTCT FANCA Gene Mutation in North of Khyber Pakhtunkhwa (KPK) Pakistan Fanconi’s Anemia Population;Iranian Journal of Pediatric Hematology & Oncology;2022-07-13