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https://www.jci.org/articles/view/118519
JCI - Induction of Fanconi anemia cellular phenotype in human 293 cells by overexpression of a...
fanconi anemia
jci
induction
cellular
phenotype
https://www.ebsco.com/research-starters/health-and-medicine/fanconi-anemia
Fanconi anemia | Health and Medicine | Research Starters | EBSCO Research
fanconi anemia
health
medicine
research
starters
https://pubmed.ncbi.nlm.nih.gov/26657402/
Fanconi anemia with biallelic FANCD1/BRCA2 mutations - Case report of a family with three affected...
Fanconi anemia, complementation group D1 with bi-allelic FANCD1 (BRCA2) mutations, is a very rare genetic disorder characterized by early onset of childhood...
fanconi anemia
case report
mutations