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August 1, 1983
Antithrombin III (AT III) Padua2: a "new" congenital abnormality with defective heparin co-factor activities but no thrombotic disease
A Girolami, F Fabris, G Cappellato, et al.
Cancer Genetics and Cytogenetics
|
May 9, 2002
Fluorescence in situ hybridization improves cytogenetic results in the analysis of hepatoblastoma
L Sainati, A Leszl, C Surace, et al.
Medical and Pediatric Oncology
|
September 14, 2002
Fluorescent in situ hybridization (FISH) reveals frequent and recurrent numerical and structural abnormalities in hepatoblastoma with no informative karyotype
C Surace, A Leszl, G Perilongo, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1988
T-cell chronic lymphocytic leukaemia: the spectrum of mature T-cell disorders
E Matutes, V Brito-Babapulle, I Worner, et al.
British Journal of Haematology
|
January 29, 2000
Features of essential thrombocythaemia in childhood: a study of five children
M L Randi, M C Putti, F Fabris, et al.
Cancer Genetics and Cytogenetics
|
December 1, 1993
A mesenchymal chondrosarcoma of a child with the reciprocal translocation (11;22)(q24;q12)
L Sainati, A Scapinello, A Montaldi, et al.
International Journal of Oncology
|
May 17, 2000
Evidence of involvement of the PLAG1 gene in lipoblastomas
A Astrom, E S D'Amore, L Sainati, et al.
Pediatric Hematology and Oncology
|
March 1, 1996
Transient acute monoblastic leukemia with reciprocal (8;16)(p11;p13) translocation
L Sainati, S Bolcato, M G Cocito, et al.
Leukemia Research
|
November 22, 2000
Deletion of parental GST genes as a possible susceptibility factor in the etiology of infant leukemia
S Garte, E Taioli, F Crosti, et al.
Blood
|
July 1, 1990
A variant form of hairy cell leukemia resistant to alpha-interferon: clinical and phenotypic characteristics of 17 patients
L Sainati, E Matutes, S Mulligan, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 27) with videos related to
Sort By:
Page
of 3
Blut
|
August 1, 1983
Antithrombin III (AT III) Padua2: a "new" congenital abnormality with defective heparin co-factor activities but no thrombotic disease
A Girolami, F Fabris, G Cappellato, et al.
Cancer Genetics and Cytogenetics
|
May 9, 2002
Fluorescence in situ hybridization improves cytogenetic results in the analysis of hepatoblastoma
L Sainati, A Leszl, C Surace, et al.
Medical and Pediatric Oncology
|
September 14, 2002
Fluorescent in situ hybridization (FISH) reveals frequent and recurrent numerical and structural abnormalities in hepatoblastoma with no informative karyotype
C Surace, A Leszl, G Perilongo, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1988
T-cell chronic lymphocytic leukaemia: the spectrum of mature T-cell disorders
E Matutes, V Brito-Babapulle, I Worner, et al.
British Journal of Haematology
|
January 29, 2000
Features of essential thrombocythaemia in childhood: a study of five children
M L Randi, M C Putti, F Fabris, et al.
Cancer Genetics and Cytogenetics
|
December 1, 1993
A mesenchymal chondrosarcoma of a child with the reciprocal translocation (11;22)(q24;q12)
L Sainati, A Scapinello, A Montaldi, et al.
International Journal of Oncology
|
May 17, 2000
Evidence of involvement of the PLAG1 gene in lipoblastomas
A Astrom, E S D'Amore, L Sainati, et al.
Pediatric Hematology and Oncology
|
March 1, 1996
Transient acute monoblastic leukemia with reciprocal (8;16)(p11;p13) translocation
L Sainati, S Bolcato, M G Cocito, et al.
Leukemia Research
|
November 22, 2000
Deletion of parental GST genes as a possible susceptibility factor in the etiology of infant leukemia
S Garte, E Taioli, F Crosti, et al.
Blood
|
July 1, 1990
A variant form of hairy cell leukemia resistant to alpha-interferon: clinical and phenotypic characteristics of 17 patients
L Sainati, E Matutes, S Mulligan, et al.
Page
of 3