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LinkedIn: Stefania Gimelli | Perfil profesional
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LinkedIn: Stefania Gimelli | Profil professionnel
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LinkedIn: Stefania Gimelli | Profilo professionale
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Interests
Researchers find new translocation; weak spots in DNA lead ...www.sciencedaily.com › releases ›
www.sciencedaily.com
... Ruediger Klaes, Georgio Gimelli, Stefania Gimelli, Robert M. Gemmill et al. A Palindrome-Mediated Recurrent Translocation with 3:1 Meiotic ...
13q Deletion and central nervous system anomalies: further insights...
jmg.bmj.com
Lucia Ballarati, Elena Rossi, Maria Teresa Bonati, Stefania Gimelli, Paola Maraschio, Palma Finelli,. Sabrina Giglio, Elisabetta Lapi, Maria Francesca Bedeschi, ...
Duplications of the critical Rubinstein–Taybi deletion region on...
jmg.bmj.com
Stefania Gimelli 2, Jean-Pierre Fryns 1, Geert Mortier 4, Jan M Friedman 9, Laurent Villard 11, ...
Business Profiles
Researchgate: Stefania Gimelli
Genève, GE, Switzerland
Education
Brief report - Research Portal, King's College, London
kclpure.kcl.ac.uk
author = "Aoife Murray and Audrey Letourneau and Claudia Canzonetta and Elisavet Stathaki and Stefania Gimelli and Frederique Sloan-Bena and Robert ...
Books & Literature
Gimelli, Stefania | Archive ouverte UNIGE
archive-ouverte.unige.ch
Archive institutionnelle de l'Université de Genève - Institutional Repository of the University of Geneva
L'Array-CGH e la sue applicazioni cliniche: tesi di dottorato ...books.google.com › books › about › L_Array_CGH_e_la_sue_applicazi...
books.google.de
L'Array-CGH e la sue applicazioni cliniche: tesi di dottorato. Front Cover. Stefania Gimelli Reviews. What people are saying - Write a review. We haven't ...
Related Documents
A rare 3q microdeletion including GAP43 and LSAMP ...www.scienceopen.com › document
www.scienceopen.com
Stefania Gimelli. Massimiliano Leoni. Maja Di Rocco. Gianluca Caridi. Simona Porta. Cristina Cuoco. Giorgio Gimelli. Elisa Tassano ...
CiteSeerX — Characterization of a recurrent 15q24 microdeletion...
citeseerx.ist.psu.edu
@MISC{Sharp07characterizationof, author = {Andrew J. Sharp and Rebecca R. Selzer and Joris A. Veltman and Stefania Gimelli and Giorgio Gimelli and Pasquale Striano ...
EBSCOhost | | De novo deletion of chromosome 11q12.3 in...
web.a.ebscohost.com
1. . Elisa Tassano Stefania Gimelli
CiteSeerX — Cryptic deletions are a common finding in ‘‘balanced’’...
citeseerx.ist.psu.edu
@MISC{Gregori07crypticdeletions, author = {Manuela De Gregori and Roberto Ciccone and Pamela Magini and Tiziano Pramparo and Stefania Gimelli and Jole Messa and ...
Scientific Publications
A Palindrome-Mediated Recurrent Translocation with 3:1 Meiotic...
www.ncbi.nlm.nih.gov
... M. Milunsky,4 Ying Zou,4 Ruediger Klaes,5 Georgio Gimelli,6Stefania Gimelli,7 Robert M. Gemmill,8 Harry A. Drabkin,8 April M. Hacker,1 Julia Brown,1 David ...
Identification of a rare 17p13.3 duplication including the BHLHA9 and...
bmcmedgenet.biomedcentral.com
Deletions and duplications of the PAFAH1B1 and YWHAE genes in 17p13.3 are associated with different clinical phenotypes. In particular, deletion of PAFAH1B1...
Brief Report: Isogenic Induced Pluripotent Stem Cell Lines From an...
www.ncbi.nlm.nih.gov
Aoife Murray, 1 , 3 Audrey Letourneau, 4 Claudia Canzonetta, 1 Elisavet Stathaki, 5Stefania Gimelli, 5 Frederique Sloan‐Bena, 5 Robert Abrehart, 1 Pollyanna ...
Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are...
molecularcytogenetics.biomedcentral.com
Since the introduction of the array-CGH technique in the diagnostic workup of mental retardation, new recurrent copy number variations and novel...
Publications
Publications Authored by Giorgio Gimelli | PubFacts
www.pubfacts.com
Publications Authored by Giorgio Gimelli
Reports & Statements
The Cancer-Causing Metal Millions Eat, Wear or Have Injected into
greenmedinfo.com
Greenmedinfo.com - Natural Health Resource - The world's most widely referenced, open access, natural medicine database, with 30,000+ study abstracts and...
nature.com search
www.nature.com
nature.com search. Login / Sign up. Showing 1–6 of 6 results. Search. advanced Stefania Gimelli, Giorgio Gimelli, Hans J. Grabe, Agnès Guichet, Olivier Guillin
Miscellaneous
Stefania Gimelli | LinkedIn
www.linkedin.com
View Stefania Gimelli’s professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Stefania Gimelli discover ...
Array comparative genomic hybridization characterization of a ...read.qxmd.com › read
read.qxmd.com
Valeria Capra, Marisol Mirabelli-Badenier, Michela Stagnaro, Andrea Rossi, Elisa Tassano, Stefania Gimelli, Giorgio Gimelli BMC Medical Genetics
Complex pathogenesis of Hirschsprung's disease in a patient ...www.rug.nl › research › portal › publications › export
research.rug.nl
author = "Paola Griseri and Yvonne Vos and Roberto Giorda and Stefania Gimelli and Silvana Beri and Giuseppe Santamaria and Guendalina Mognato and ...
[PDF] Brief Report: Isogenic Induced Pluripotent Stem Cell Lines From...
www.semanticscholar.org
AOIFE MURRAY,a,b AUDREY LETOURNEAU,c CLAUDIA CANZONETTA,a ELISAVET STATHAKI,d. STEFANIA GIMELLI,d FREDERIQUE SLOAN–BENA,d ...
Congenital Aural Atresia Associated With Agenesis of Internal Carotid...
researchportal.helsinki.fi
Elisa Tassano, Vidhya Jagannathan, Cord Drogemuller, Massimiliano Leoni, Marjo K. Hytonen, Mariasavina Severino, Stefania Gimelli, Cristina Cuoco, Maja Di ...
E-GEOD RNA-seq of induced pluripotent stem cells from...
www.omicsdi.org
... Frederique Bena Stylianos E Antonarakis Anis Feki Audrey Letourneau Sophie Dahoun Stefania Gimelli M.Reza Sailani Michel Guipponi Federico A Santoni.
E-GEOD < Browse < ArrayExpress < EMBL-EBIwww.ebi.ac.uk › arrayexpress › experiments › E-GEOD
www.ebi.ac.uk
EMBL-EBI
Detailed phenotype-genotype study in five patients with chromosome...
research.rug.nl
author = "Bonaglia, {Maria Clara} and Roberto Ciccone and Giorgio Gimelli and Stefania Gimelli and Susan Marelli and Joke Verheij and Roberto Giorda and ...
FISH results.
figshare.com
... Luisa Garrè Paolo Nozza Carlotta Vaccari Lara Bricco Frédérique Sloan-Béna Stefania Gimelli Cristina Cuoco Giorgio Gimelli Elisa Tassano.
Dr. Dengg - Zitate
www.draloisdengg.at
André-Pascal Sappino, Raphaële Buser, Laurence Lesne, Stefania Gimelli, Frédérique Béna, Dominique Belin, Stefano J. Mandriota: "Aluminium chloride ...
Identification of a rare 17p13.3 duplication Altmetricwww.altmetric.com › details
www.altmetric.com
Pubmed ID Authors. Valeria Capra, Marisol Mirabelli-Badenier, Michela Stagnaro, Andrea Rossi, Elisa Tassano, Stefania Gimelli, Giorgio Gimelli.
Interstitial 7q31.1 copy number variations disrupting IMMP2L ...cyberleninka.org › article
cyberleninka.org
Similar topics of scientific paper in Clinical medicine , author of scholarly article — Stefania Gimelli, Valeria Capra, Maja Di Rocco, Massimiliano Leoni, Marisol ...
De novo deletion of chromosome 11q12.3 in monozygotic twins affected...
moh-it.pure.elsevier.com
Carlotta M. Vaccari ; Maria V. Romanini ; Ilaria Musante ; Elisa Tassano; Stefania Gimelli ; Maria T. Divizia; Michele Torre; Carmen G. Morovic ; ...
Microarray based analysis of an inherited terminal 3p26.3 deletion,...
go.gale.com
Authors: Cristina Cuoco [1]; Patrizia Ronchetto [1]; Stefania Gimelli [2]; Frédérique Béna [2]; Maria Teresa Divizia [3]; Margherita Lerone [3]; Marisol ...
Molecular Mechanisms Generating and Stabilizing Terminal 22q13...
figshare.com
Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome
Molecular and clinical characterization of 25 individuals with exonic...
hal.archives-ouvertes.fr
Frédérique Béna 1 Damien L Bruno Mats Eriksson Conny van Ravenswaaij-Arts 2 Zornitza Stark 3 Trijnie Dijkhuizen 2 Erica Gerkes 2Stefania Gimelli 1, ...
The breakpoint identified in a balanced de novo translocation...
moh-it.pure.elsevier.com
Emanuele Panza, Giorgio Gimelli, Mario Passalacqua, Amnon Cohen, Stefania Gimelli, Sabrina Giglio, Cristina Ghezzi, Bianca Sparatore, Babett Heye, Orsetta Zuffardi ...
Molecular characterization of a t(2;6) balanced translocation that is...
moh-it.pure.elsevier.com
Renata Bocciardi, Roberto Giorda, Valeria Marigo, Paola Zordan, Donatella Montanaro, Stefania Gimelli, Marco Seri, Margherita Lerone, Roberto Ravazzolo, ...
Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are...
www.semanticscholar.org
BackgroundSince the introduction of the array-CGH technique in the diagnostic workup of mental retardation, new recurrent copy number variations and novel...
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