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of 2
pro vyhledávání: '"Leonarda lanzano"'
Autor:
Marta Centra, Leopoldo Zelante, Leonarda lanzano, Manuel Buchwald, Gian Pio de Cillis, Anna Savoia
Publikováno v:
Human Molecular Genetics. 4:1321-1326
Fanconi anaemia (FA) is an autosomal recessive disease characterised by progressive pancytopenia, chromosome instability and an increased risk of cancer. The Fanconi Anaemia Complementation Group C (FACC) gene is mutated in patients of complementatio
Autor:
Leopoldo Zelante, Sinoula Apostolou, Peter C. Verlander, Elna W. Moerland, Douglas F. Easton, Maria Savino, Alex J. Tipping, Gregory G. Lennon, Leonarda lanzano, Neil V. Morgan, Anne-Marie Cleton-Jansen, S.A. Whitmore, Larry L. Deaven, Tamar Erlich, David F. Callen, Sheila Hassock, Christopher G. Mathew, Arleen D. Auerbach, Orna Levran, Joanna Crawford, Anna Savoia, Norman A. Doggett, Maria D'Apolito, Robert K. Moyzis, Thomy J. L. de Ravel, Jan C. Pronk, Stander Jansen, Rachel A. Gibson, Sat Dev Batish, Carola Van Berkell, Elena Memeo, Grant R. Sutherland, Angelo Notarangeio, Maria Rosaria Piemontese, Cees J. Cornelisse
Publikováno v:
Nature genetics. 14(3)
The Fanconi anaemia/Breast cancer consortium* Fanconi anaemia (FA) is an autosomal recessive disorder associated with progressive bone-marrow failure, a variety of congenital abnormalities, and predisposition to acute myeloid leukaemia1. Cells from F