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Showing results (11-20 of 19) with videos related to

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Biochemical and Biophysical Research Communications|July 13, 2000
Spectrin changes occur in erythrocytes from patients with Fanconi's anemia and their parentsE Straface, R Masella, D Del Principe, et al.
FEBS Letters|June 16, 1997
Resistance to apoptosis in Fanconi's anaemia. An ex vivo study in peripheral blood mononuclear cellsD Monti, S Macchioni, M Guido, et al.
FEBS Letters|February 29, 2000
Cytoskeleton alterations of erythrocytes from patients with Fanconi's anemiaW Malorni, E Straface, G Pagano, et al.
Human Genetics|January 1, 1997
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A geneA Savoia, M R Piemontese, M Savino, et al.
Leukemia|November 11, 2006
A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemiaA Borriello, A Locasciulli, A M Bianco, et al.
Medical Hypotheses|October 29, 1998
Congenital disorders sharing oxidative stress and cancer proneness as phenotypic hallmarks: prospects for joint research in pharmacologyG Pagano, L G Korkina, U T Brunk, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9I Demuth, M Wlodarski, A J Tipping, et al.
Blood|December 9, 2000
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research GroupL Faivre, P Guardiola, C Lewis, et al.
Journal of Medical Genetics|September 4, 2007
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patientsM De Gregori, R Ciccone, P Magini, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Biochemical and Biophysical Research Communications|July 13, 2000
Spectrin changes occur in erythrocytes from patients with Fanconi's anemia and their parentsE Straface, R Masella, D Del Principe, et al.
FEBS Letters|June 16, 1997
Resistance to apoptosis in Fanconi's anaemia. An ex vivo study in peripheral blood mononuclear cellsD Monti, S Macchioni, M Guido, et al.
FEBS Letters|February 29, 2000
Cytoskeleton alterations of erythrocytes from patients with Fanconi's anemiaW Malorni, E Straface, G Pagano, et al.
Human Genetics|January 1, 1997
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A geneA Savoia, M R Piemontese, M Savino, et al.
Leukemia|November 11, 2006
A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemiaA Borriello, A Locasciulli, A M Bianco, et al.
Medical Hypotheses|October 29, 1998
Congenital disorders sharing oxidative stress and cancer proneness as phenotypic hallmarks: prospects for joint research in pharmacologyG Pagano, L G Korkina, U T Brunk, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9I Demuth, M Wlodarski, A J Tipping, et al.
Blood|December 9, 2000
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research GroupL Faivre, P Guardiola, C Lewis, et al.
Journal of Medical Genetics|September 4, 2007
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patientsM De Gregori, R Ciccone, P Magini, et al.
Pageof 2