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Mostrati risultati da 1 a 20 di 57
Titolo Data di pubblicazione Autori Tipo File Abstract
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR 1999 L. CorradoP. ColapietroL. LarizzaP. Riva Article (author) -
Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 1999 P. ColapietroP. RivaL.N. RossiL. Larizza + Article (author) -
Genotype-phenotype correlation in patients with NF1 microdeletion syndrome : identification of candidate genes for mental retardation 2002 P. RivaM. VenturinF. OrzanC. GervasiniP. ColapietroL. Larizza + Article (author) -
NF1 exon 7 skipping by disruption of exonic splice enhancers (ESEs) in neurofibromatosis 1 2003 P. ColapietroC. GervasiniP. RivaL. Larizza + Article (author) -
High resolution FISH analysis of NF1 REP and non-REP microdeletions evidences nonhomologous end joining mediated rearrangements 2003 P. RivaM. VenturinC. GervasiniP. ColapietroL. Larizza + Article (author) -
High resolution FISH analysis of NF1 REP and non-REP microdeletions evidences nonhomologous end joining mediated rearrangements 2003 P. RivaM. VenturinC. GervasiniP. ColapietroL. Larizza + Article (author) -
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions 2004 M. VenturinC. GervasiniF. OrzanP. ColapietroL. LarizzaP. Riva + Article (author) -
Smith-Magenis sindrome and growth hormone deficiency 2004 P. ColapietroL. Larizza + Article (author) -
KIT activating mutations : incidence in adult and pediatric AML, and identification of an internal tandem duplication 2004 A. BeghiniP. ColapietroL. Larizza + Article (author) -
Distinct expression pattern of microtubule-associated protein/microtubule affinity-regulating kinase 4 in differentiated neurons 2006 S. De BiasiP. ColapietroL. LarizzaA. Beghini + Article (author) -
Prognostic impact of c-KIT mutations in core binding factor leukemias. an Italian retrospective study 2006 A. BeghiniP. ColapietroL. Larizza + Article (author) -
Rubinstein-Taybi syndrome : spectrum of CREBBP mutations in Italian patients. 2006 C. GervasiniP. CastronovoMOTTADELLI, FEDERICAS. ManziniP. ColapietroL. Larizza + Article (author) -
Serum tryptase levels in AML at diagnosis : a multicenter retrospective study 2006 A. BeghiniP. Colapietro + Article (author) -
KIT mutations in core binding factor leukemias: outcome prediction and therapeutic implications 2006 A. BeghiniP. ColapietroL. Larizza + Article (author) -
Molecular screening of PDGFRA and PDGFRB genes in KIT and FLT3 negative core binding factor leukemias 2007 A. BeghiniP. Colapietro + Article (author) -
Prevalence and prognostic impact of KIT mutations in acute myeloid leukaemia with inv(16). A retrospective study 2007 A. BeghiniP. Colapietro + Article (author) -
IMPACT OF KIT MUTATIONS IN ACUTE MYELOID LEUKAEMIA WITH INV(16) 2008 A. BeghiniP. Colapietro + Article (author) -
Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorphism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation 2008 Beghini A.Colapietro P. + Article (author) -
Altered H19 and SNAT2 expression in type 1 IUGR (Intrauterine Growth Restriction) placentas 2008 S. TabanoC. MandòP. ColapietroS. CalabreseP. PileriV. SignorelliM.R. MiozzoI. Cetin + Article (author) -
Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorfism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation 2008 A. BeghiniP. Colapietro + Article (author) -
Mostrati risultati da 1 a 20 di 57
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