Skip to search formSkip to main contentSkip to account menu

FANCONI ANEMIA, COMPLEMENTATION GROUP T

Known as: FANCT 
National Institutes of Health

Related topics

Related topics

8 relations
AnemiaAutosomal recessive inheritanceDuplication of thumb phalanxHypoplasia of thumb

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
FANCL gene mutations in premature ovarian insufficiency
The Fanconi anemia (FA) pathway is mainly involved in DNA interstrand crosslinks (ICLs) repair in the genome. Several FA genes… 
2017
2017
A novel system for detection of DNA double strand breaks and repair in human cells
2016
2016
The Simple Chordate Ciona intestinalis Has a Reduced Complement of Genes Associated with Fanconi Anemia
Fanconi anemia (FA) is a human genetic disease characterized by congenital defects, bone marrow failure, and increased cancer… 
Review
2016
Review
2016
[Inherited bone marrow failure syndromes].
Inherited bone marrow failure syndromes comprise a series of disorders caused by various gene mutations. Genetic tests were… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)