M. Angioletti

发表

Use of Single-Value Protein Compensation of the Jaffe Creatinine Assay Contributes to Clinically Significant Inaccuracy in Results

M. Pistillo, M. Venturini, P. Piccioli, 2007 .

In vivo gene marking of rhesus macaque long‐term repopulating hematopoietic cells using a VSV‐G pseudotyped versus amphotropic oncoretroviral vector

L. Luzzatto, C. Dunbar, R. Donahue, 2004, The journal of gene medicine.

Identification and molecular characterization of a novel 55‐kb deletion recurrent in southern Italy: the Italian Gγ(Aγδβ)°‐thalassemia

G. Piluso, L. Mastrullo, G. Lacerra, 2013, European journal of haematology.

Hemoglobin Neapolis, p126(H4)Val + Gly: A Novel f3-Chain Variant Associated With a Mild P-Thalassemia Phenotype and Displaying Anomalous Stability Features

L. Camardella, G. Lacerra, C. Carestia, 2003 .

Recent advances in pathogenesis of paroxysmal nocturnal hemoglobinuria

R. Notaro, L. Gargiulo, M. Sica, 2015 .

Multiplex Tetra-Primer Amplification Refractory Muta- tion System PCR to Detect 6 Common Germline Muta- tions of the MUTYH Gene Associated with Polyposis

V. Gismondi, P. Piccioli, M. Serra, 2006 .

( a ) d 3 : A Novel a +-Thalassemia Deletion With the Breakpoints in the a 2-Globin Gene and in Close Proximity to an A h Family Repeat Between the 3 ra 2-and * al-Globin Genes

G. Lacerra, C. Carestia, A. Viola, 2003 .

ααααanti-3.7 type II: a new α-globin gene rearrangement suggesting that the α-globin gene duplication could be caused by intrachromosomal recombination

C. D. Bonis, G. Buonanno, G. Lacerra, 1992, Human Genetics.

(Alpha)alpha 5.3: a novel alpha(+)-thalassemia deletion with the breakpoints in the alpha 2-globin gene and in close proximity to an Alu family repeat between the psi alpha 2- and psi alpha 1-globin genes

C. D. Bonis, G. Lacerra, A. Viola, 1991 .

Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features

L. Mastrullo, G. Lacerra, C. Gaudiano, 2002, Human mutation.

Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants

Margherita Berardi, A. Spurdle, M. Genuardi, 2017, Human mutation.

CD59 Deficiency Is Critical for C3 Binding on Red Blood Cells of Patients with Paroxysmal Nocturnal Hemoglobinuria (PNH) during Anti-C5 Treatment (eculizumab)

A. Risitano, R. Notaro, P. Ricci, 2016 .

β-globin gene framework variant: an African type?

C. D. Bonis, G. Lacerra, C. Carestia, 1991 .

Overexpression of ETV4 is oncogenic in prostate cells through promotion of both cell proliferation and epithelial to mesenchymal transition

R. Notaro, C. Luceri, M. Sica, 2012, Oncogenesis.

Hemoglobin Neapolis, beta 126(H4)Val----Gly: a novel beta-chain variant associated with a mild beta-thalassemia phenotype and displaying anomalous stability features.

L. Camardella, G. Lacerra, A. Viola, 1991, Blood.