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Fanconi Anemia Pages on BioPortfolio:
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BioPortfolio.com - BioWeb Aplastic Anemia Search
Synonyms Fanconi's Anemia, Type I (FA1) Fanconi Pancytopenia Fanconi's Anemia, Estren-Dameshek Variant Aplastic Anemia with Congenital Anomalies Congenital ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...
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BioPortfolio - FANCD2 - Fanconi anemia, complementation group D2
Each of the thirteen identified Fanconi anemia (FA) genes is required for. ... Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to ...
http://www.bioportfolio.com/gene/2177-FANCD2.html...
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BioPortfolio - FANCI - Fanconi anemia, complementation group I
First, KIAA1794 is a Fanconi anemia gene. Second, this gene is identical to ... Each of the thirteen identified Fanconi anemia (FA) genes is required for. ...
http://www.bioportfolio.com/gene/55215-FANCI.html...
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BioPortfolio - FANCA - Fanconi anemia, complementation group A
Cellular and molecular consequences of defective Fanconi anemia proteins in ... Fanconi anemia protein FANCF forms a nuclear complex with FANCA, ...
http://www.bioportfolio.com/gene/2175-FANCA.html...
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BioPortfolio - FANCL - Fanconi anemia, complementation group L
Cellular and molecular consequences of defective Fanconi anemia proteins in ... Fanconi anemia (FA) is a rare autosomal recessive or X-linked disorder. ...
http://www.bioportfolio.com/gene/55120-FANCL.html...
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BioPortfolio - FANCF - Fanconi anemia, complementation group F
Fanconi anemia (FA) is a rare autosomal recessive or X-linked disorder. ... A possible approach for stem cell gene therapy of Fanconi anemia. ...
http://www.bioportfolio.com/gene/2188-FANCF.html...
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BioPortfolio - Fanconi Anemia
Fanconi Anemia Complementation Group FANCD2 Protein Serine 331 Phosphorylation Is Important for Fanconi Anemia Pathway Function and BRCA2 Interaction. ...
http://www.bioportfolio.com/indepth/Fanconi_Anemia.html...
| Results from other life science and pharmaceutical sites:
Fanconi anemia - Wikipedia, the free encyclopedia
Fanconi anemia (FA) is a genetic disease that affects children and adults from all ethnic backgrounds. The disease is named after the Swiss pediatrician who
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http://en.wikipedia.org/wiki/Fanconi_anemia...
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Fanconi Anemia, What Is
Fanconi anemia (fan-KO-nee uh-NEE-me-uh), or FA, is a rare, inherited blood disorder that leads to bone marrow failure.
http://www.nhlbi.nih.gov/health/dci/Diseases/fanconi/fanconi...
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Fanconi's anemia: MedlinePlus Medical Encyclopedia
21 Sep 2009 ... Fanconi's anemia is disease passed down through families (inherited) that mainly affects the bone marrow. It results in decreased production ...
http://www.nlm.nih.gov/medlineplus/ency/article/000334.htm...
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OMIM - FANCONI ANEMIA; FA
Fanconi ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650...
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Fanconi Anemia, Treatment
Doctors decide how to treat Fanconi anemia (FA) based on a patient's age and how well (or how poorly) the patient's bone marrow is producing new blood ...
http://www.nhlbi.nih.gov/health/dci/Diseases/fanconi/fanconi...
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The Rockefeller University - Fanconi Anemia Mutation Database
The Fanconi Anemia Mutation Database was established in 1998 as a cooperative effort to accelerate the availability of information on mutations in these ...
http://www.rockefeller.edu/fanconi/mutate/...
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Fanconi Anemia, Diagnosis
People who have Fanconi anemia (FA) are born with the disease. They may or may not show signs or symptoms of it at birth.
http://www.nhlbi.nih.gov/health/dci/Diseases/fanconi/fanconi...
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Fanconi Anemia -- GeneReviews -- NCBI Bookshelf
Fanconi anemia (FA) is characterized by physical abnormalities, bone marrow failure, and increased risk of malignancy. Physical abnormalities, present in
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http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
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Fanconi Anemia, Causes
Fanconi anemia (FA) is an inherited disease. “Inherited” means that the disease is passed from parents to children through abnormal genes. ...
http://www.nhlbi.nih.gov/health/dci/Diseases/fanconi/fanconi...
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Fanconi anemia.
Fanconi anemia (FA) is a rare hereditary disease characterized by bone marrow failure and developmental anomalies; a high incidence of myelodysplasia (MDS),
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http://www.ncbi.nlm.nih.gov/pubmed/16822457...
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