FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Giulia Arrigo

Research Profile

Procedures

Anatomy

X Chromosome

Concepts & Ideas

Chemicals & Drugs

Disorders

Genes & Molecular Sequences

Co-author Network

Publications

TOP 3
Annalisa Vetro; Giulia Arrigo; Stefania Cesari; Gianfranco Croci; Barbara Dal Bello; Fabrizia Franchi; Angela Iasci; Thomas Liehr; Emmanouil Manolakos; Maria Marinelli; Emanuela Meneghelli; Michael B Petersen; Loretta Thomaidis; Orsetta Zuffardi
Unexpected results in the constitution of small supernumerary marker chromosomes.
Lucia Ballarati; Elena Rossi; Maria Teresa Bonati; stefania gimelli; Paola Maraschio; Palma Finelli; Sabrina Giglio; Elisabetta Lapi; Maria Francesca Bedeschi; Silvana Guerneri; Giulia Arrigo; Maria Grazia Patricelli; Teresa Mattina; Oriana Guzzardi; Vanna Pecile; Adalgisa Police; Gioacchino Scarano; Lidia Larizza; Orsetta Zuffardi; Daniela Giardino
13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.
Sabrina Giglio; Barbara Pirola; Giulia Arrigo; P Dagrada; Barbara Bardoni; F Bernardi; G Russo; L Argentiero; Antonino Forabosco; Rosalba Carrozzo; Orsetta Zuffardi
Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Giulia Arrigo (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Annalisa Vetro; Giulia Arrigo; Stefania Cesari; Gianfranco Croci; Barbara Dal Bello; Fabrizia Franchi; Angela Iasci; Thomas Liehr; Emmanouil Manolakos; Maria Marinelli; Emanuela Meneghelli; Michael B Petersen; Loretta Thomaidis; Orsetta Zuffardi
Unexpected results in the constitution of small supernumerary marker chromosomes.
European journal of medical genetics 2012;55(3):185-90.
2007: Lucia Ballarati; Elena Rossi; Maria Teresa Bonati; stefania gimelli; Paola Maraschio; Palma Finelli; Sabrina Giglio; Elisabetta Lapi; Maria Francesca Bedeschi; Silvana Guerneri; Giulia Arrigo; Maria Grazia Patricelli; Teresa Mattina; Oriana Guzzardi; Vanna Pecile; Adalgisa Police; Gioacchino Scarano; Lidia Larizza; Orsetta Zuffardi; Daniela Giardino
13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.
Journal of medical genetics 2007;44(1):e60.
2000: Sabrina Giglio; Barbara Pirola; Giulia Arrigo; P Dagrada; Barbara Bardoni; F Bernardi; G Russo; L Argentiero; Antonino Forabosco; Rosalba Carrozzo; Orsetta Zuffardi
Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements.
European journal of human genetics : EJHG 2000;8(1):63-70.
1999: S Rivella; B Palermo; C Pelizon; Cinzia Sala; Giulia Arrigo; Daniela Toniolo
Selection and mapping of replication origins from a 500-kb region of the human X chromosome and their relationship to gene expression.
Genomics 1999;62(1):11-20.
1999: A Fogli; Sabrina Giglio; Giulia Arrigo; Cristiana Lo Nigro; Massimo Zollo; Luigi Viggiano; Mariano Rocchi; Nicoletta Archidiacono; Orsetta Zuffardi; Rosalba Carrozzo
Identification of two paralogous regions mapping to the short and long arms of human chromosome 2 comprising LIS1 pseudogenes.
Cytogenetics and cell genetics 1999;86(3-4):225-32.
1998: Francesca Sanvito; Giulia Arrigo; Orsetta Zuffardi; M Agnelli; Pier Carlo Marchisio; Stefano Biffo
Localization of p27 beta 4 binding protein gene (ITGB4BP) to human chromosome region 20q11.2.
Genomics 1998;52(1):111-2.
1998: Francesca Moro; Giulia Arrigo; A Fogli; L Bernard; Rosalba Carrozzo
The beta and gamma subunits of the human platelet-activating factor acetyl hydrolase isoform Ib (PAFAH1B2 and PAFAH1B3) map to chromosome 11q23 and 19q13.1, respectively.
Genomics 1998;51(1):157-9.
1998: Silvia Bione; Cinzia Sala; C Manzini; Giulia Arrigo; Orsetta Zuffardi; S Banfi; Giuseppe Borsani; P Jonveaux; C Philippe; Maurizio Zuccotti; Andrea Ballabio; Daniela Toniolo
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility.
American journal of human genetics 1998;62(3):533-41.
1998: L Dal Zotto; NA Quaderi; R Elliott; P A Lingerfelter; Laura Carrel; V Valsecchi; Eugenio Montini; C H Yen; Verne M Chapman; I Kalcheva; Giulia Arrigo; Orsetta Zuffardi; S Thomas; Huntington F Willard; Andrea Ballabio; Christine M Disteche; Elena I Rugarli
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region.
Human molecular genetics 1998;7(3):489-99.
1998: P Fumagalli; M Accarino; Aliana Egeo; Paolo Scartezzini; G Rappazzo; Antonio Pizzuti; V Avvantaggiato; A Simeone; Giulia Arrigo; Orsetta Zuffardi; Sergio Ottolenghi; Roberto Taramelli
Human NRD convertase: a highly conserved metalloendopeptidase expressed at specific sites during development and in adult tissues.
Genomics 1998;47(2):238-45.
1997: Rosalba Carrozzo; Giulia Arrigo; E Rossi; Barbara Bardoni; M Cammarata; P Gandullia; R Gatti; Orsetta Zuffardi
Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivation.
American journal of medical genetics 1997;72(3):329-34.
1997: Cinzia Sala; Giulia Arrigo; G Torri; F Martinazzi; P Riva; Lidia Larizza; C Philippe; P Jonveaux; F Sloan; T Labella; Daniela Toniolo
Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21.
Genomics 1997;40(1):123-31.
1997: Giulia Arrigo; Roberto Gherzi; Maria Clara Bonaglia; Alessandra Leprini; Orsetta Zuffardi; Luciano Zardi
Assignment of the tenascin-R gene (Tnr) to mouse chromosome 4 band E2 by fluorescence in situ hybridization; refinement of the human TNR location to chromosome 1q24.
Cytogenetics and cell genetics 1997;78(2):145-6.
1996: N Mastroianni; Maurizio De Fusco; Massimo Zollo; Giulia Arrigo; Orsetta Zuffardi; Alberto Bettinelli; A Ballabio; Giorgio Casari
Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3).
Genomics 1996;35(3):486-93.