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Browsing by Author Pasquali F
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Showing results 1 to 7 of 7
Issue Date
Title
Author(s)
2007
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies
Maserati E
;
Pressato B
;
Valli R
;
Patitucci F
;
Lo Curto F
;
Pasquali F
;
Minelli A
;
Danesino C
;
Marchetti M
;
Barosi G
2004
Familial myelodysplastic syndromes monosomy 7/trisomy 8 and mutator effects
Maserati E
;
Minelli A
;
Menna G
;
Cecchini MP
;
Bernardo ME
;
Rossi G
;
De Filippi P
;
Lo Curto F
;
Danesino C
;
Locatelli F
;
Pasquali F
2004
Familial platelet disorder with propensity to acute myelogenous leukemia: Genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies
Minelli A
;
Maserati E
;
Rossi G
;
Bernardo ME
;
De Stefano P
;
Cecchini MP
;
Valli R
;
Albano V
;
Pierani P
;
Leszl A
;
Sainati L
;
Lo Curto F
;
Danesino C
;
Locatelli F
;
Pasquali F
2004
HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t(5,17)(q33,p112)
Morerio C
;
Acquila M
;
Rosanda C
;
Rapella A
;
Dufour C
;
Locatelli F
;
Maserati E
;
Pasquali F
;
Panarello C
2007
Monitoring the lsochromosome i(7)(q10) in the bone marrow of patients with Shwachman syndrome by real-time quantitative PCR
Porta G
;
Mattarucchi E
;
Maserati E
;
Pressato B
;
Valli R
;
Morerio C
;
Zecca M
;
Panarello C
;
Locatelli F
;
Lo Curto F
;
Pasquali F
2007
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR
Porta G
;
Maserati E
;
Mattarucchi E
;
Minelli A
;
Pressato B
;
Valli R
;
Zecca M
;
Bernardo ME
;
Lo Curto F
;
Locatelli F
;
Danesino C
;
Pasquali F
2006
Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies
Maserati E
;
Minelli A
;
Pressato B
;
Valli R
;
Crescenzi B
;
Stefanelli M
;
Menna G
;
Sainati L
;
Poli F
;
Panarello C
;
Zecca M
;
Lo Curto F
;
Mecucci C
;
Danesino C
;
Pasquali F
Showing results 1 to 7 of 7
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