Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Pushpa Vasudevan"'
Autor:
Charmaine Havenga, Neil V. Morgan, Ian C. Pearson, Atieh Hajianpour, Judith C. W. Marsh, Laura H. Goldstein, Christopher G. Mathew, M. Murer-Orlando, Nicola Foot, Farkondeh Birjandi, Sheila P. Mohan, Thomas Pearson, Elena Samochatova, Rachel A. Gibson, Irene Roberts, Inderjeet Dokal, Juan C. Llerena, Richard J. Cohn, R. David Milner, Thomy J. L. de Ravel, Sarah E. Ball, Stander Jansen, Isabel M. Marques, Pushpa Vasudevan, I Kesterton
Fanconi anemia (FA) is an autosomal recessive disorder associated with hypersensitivity to DNA cross-linking agents and bone marrow failure. At least four complementation groups have been defined, and the FA group C gene (FAC) has been cloned. We hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::601451df0deb90420c7ce36a9618b13d
https://doi.org/10.1002/(sici)1098-1004(1996)8:2<140::aid-humu6>3.0.co
https://doi.org/10.1002/(sici)1098-1004(1996)8:2<140::aid-humu6>3.0.co
Autor:
Gibson, Rachel A., Morgan, Neil V., Goldstein, Laura H., Pearson, Ian C., Kesterton, Ian P., Foot, Nicola J., Jansen, Stander, Havenga, Charmaine, Pearson, Thomas, de Ravel, Thomy J., Cohn, Richard J., Marques, Isabel M., Dokal, Inderjeet, Roberts, Irene, Marsh, Judith, Ball, Sarah, Milner, R. David, Llerena, Juan C., Samochatova, Elena, Mohan, Sheila P.
Publikováno v:
Human Mutation; 1996, Vol. 8 Issue 2, p140-148, 9p
