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FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
Known as:
FANCONI ANEMIA, COMPLEMENTATION GROUP A
, FA
, FANCA
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Fanconi anemia caused by mutations of the FANCA gene. FANCA gene mutations are the most common cause of Fanconi anemia. This gene provides…
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National Institutes of Health
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Related topics
Related topics
30 relations
Abnormal renal morphology
Anemia
Anemic pallor
Autosomal recessive inheritance
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Analysis of overlapping CNVs and two FANCA-VPS9D1 fusion transcripts in a Fanconi anemia patient
Jing Zhang
2019
Corpus ID: 214216505
2019
2019
FANCA Gene in Pakistani Fanconi Anemia Patients: Screening of Mutations in Exon 28 and Exon 29
Saima Iram
,
Iram Aftab
,
+5 authors
S. Mohsin
2019
Corpus ID: 212520841
Objective: This kind of study was conducted first time in Pakistan. Its objective was to ascertain the associated clinical…
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2018
2018
2 Inflammatory ROS in Fanconi Anemia Hematopoiesis and Leukemogenesis
2018
Corpus ID: 53598097
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure (BMF), clonal proliferation of hematopoietic stem…
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2017
2017
Therapeutic research in fanconi anemia
Helena Montanuy Escribano
2017
Corpus ID: 208405596
Much effort is being made on Fanconi anemia therapeutics to treat bone marrow failure and cancer, the most life threatening signs…
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2015
2015
Cross talk between fanconi anemia and unc5a signaling pathway
FengFei Huang
2015
Corpus ID: 91004413
L’anemie de Fanconi (AF) est une maladie infantile multigenique et complexe. Les enfants atteints d’AF souffrent d’une…
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2013
2013
FANCA and FANCG are the major Fanconi anemia genes in the Korean population
J. Parka
,
N-G Chungb
,
+4 authors
IY Parkc
2013
Corpus ID: 32250576
Fanconi anemia (FA) is a rare disorder characterized by physical abnormalities, bone marrow failure (BMF), increased risk of…
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2012
2012
Inflammatory ROS in Fanconi Anemia Hematopoiesis and Leukemogenesis
2012
Corpus ID: 35183933
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure (BMF), clonal proliferation of hematopoietic stem…
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2005
2005
Fluorescence in situ hybridization as a diagnostic tool for the detection of the FANCA delE12-31 and delE11-17 mutations
Sibongile Joy Nogabe
2005
Corpus ID: 90723446
2002
2002
Molecular Bio logy Ser ies The Molecular Biology of Fanconi Anemia
H. Tamary
,
R. Bar-Yam
,
M. Zemach
,
O. Dgany
,
L. Shalmon
,
I. Yaniv
2002
Corpus ID: 39944385
Fanconi anemia is a rare autosomal recessive disorder characterized clinically by congenital abnormalities, progressive bone…
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1999
1999
Fiche no. 30: Fanca (anémie de Fanconi de type A). Gène de réparation?
T. Soussi
1999
Corpus ID: 78508390