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Vanna Pecile parla di genetica all'osservatorio di Farra - Il Piccolo ...
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FARRA. “Genetica umana: nuove frontiere e nuove sfide”. È il titolo della conferenza che la dottoressa Vanna Pecile, dirigente biologo con ...
La dottoressa Vanna Pecile parla di genetica medica - Messaggero...
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FAGAGNA. Stasera, alle 20,30, nella sala consiliare si parlerà di genetica medica: la serata, organizzata dal Centro italiano femminile insieme al...
Network Profiles
LinkedIn: Vanna Pecile | LinkedIn
Visualizza il profilo professionale di Vanna Pecile su LinkedIn. LinkedIn è la rete professionale più grande al mondo utilizzata dai professionisti come Vanna ...
Interests
Just a moment...
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Vanna Pecile 3, Andrea Riccio 2, 4, Giovanni Neri 1; 1 Istituto di Genetica Medica, Università Cattolica Sacro Cuore, Policlinico “A.Gemelli”, Roma, Italy ...
Business Profiles
Researchgate: Vanna Pecile
Trieste, Friuli Venezia Giulia, Italy
Books & Literature
Vanna Pecile | OMICS International
www.longdom.org
Biography. He currently works at Laboratory of Medical Genetics, Institute for Maternal and Child Health-IRCCS “Burlo Garofolo” Trieste, Italy. Research Interest. Medical Genetics,Maternal and Child Health. Publications. Chromothripsis in Lipoblastoma. Federica Pederiva, Vanessa Candilera, Lisa Cleva and Vanna Pecile.
authors:"Vanna Pecile" - Search | Paperity
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Paperity: the 1st multidisciplinary aggregator of Open Access journals & papers. Free fulltext PDF articles from hundreds of disciplines, all in one place
Vanna Pecile | XanEdu Customization Platform
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Author: Vanna Pecile. Results. A new case of duplication of the MDS region identified by high-density SNP arrays and a review of the literature Springer ...
Related Documents
CiteSeerX — ELECTRONIC LETTER 13q Deletion and central nervous system...
citeseerx.ist.psu.edu
... Bedeschi and Silvana Guerneri and Giulia Arrigo and Grazia Patricelli and Teresa Mattina and Oriana Guzzardi and Vanna Pecile and Adalgisa Police and Lidia ...
A multi-method approach to the molecular diagnosis of overt and...
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Giovanni Battista Ferrero: . Vanna Pecile: .it. Lidia Larizza: ...
CiteSeerX — JOURNAL OF MEDICAL CASE REPORTS
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@MISC{Travan_journalof, author = {Laura Travan and Vanna Pecile and Mariacristina Fertz and Antonella Fabretto and Pierpaolo Brovedani and Sergio Demarini and John …
Copy number variations in the X chromosome of Klinefelter syndrome
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Copy number variations in the X chromosome of Klinefelter syndrome Alberto Ferlin 1, Maria Santa Rocca 1, Vanna Pecile 2, Riccardo Selice 1, Nicola Caretta 1 & Carlo ...
Scientific Publications
Gene | Vol 565, Iss 1, Pgs , (1 July …
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FH associated 12 gene variants have been identified using NGS Ion ... Vanna Pecile, Aldo Skabar, Antonella Fabretto; Abstract; Close research highlights PDF (
Opitz trigonocephaly syndrome presenting with sudden unexplained...
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Vanna Pecile 2, Mariacristina Fertz 1, Antonella Fabretto 2, Pierpaolo Brovedani 1, ... John M Opitz 3; Journal of Medical Case Reports :222. DOI:
Further phenotype description, genotype characterization in patients ...
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Related Researchers. Calculating key researchers relating to this paper. Vanna Pecile. Researcher. Claudia A L Ruivenkamp. Researcher.
European Journal of Medical Genetics | Vol 56, Iss 1, Pgs
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Pages ; Maria Santa Rocca, Flavio Faletra, Raffaella Devescovi, Paolo Gasparini, Vanna Pecile. Abstract; Close graphical abstract; PDF (381 K).
Publications
Opitz trigonocephaly syndrome presenting with sudden unexplained...
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By Laura Travan, Vanna Pecile, Mariacristina Fertz, Antonella Fabretto, Pierpaolo Brovedani, Sergio Demarini, John M Opitz and Laura Travan. Publisher: The ...
Publications Authored by Vanna Pecile | PubFacts
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Publications by authors named "Vanna Pecile". Are you Vanna Pecile? Register this Author. 40Publications. 382Reads. -Profile Views ...
IJMS | Free Full-Text | Rothmund-Thomson Syndrome: Insights from ...
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Vanna Pecile 11. and Lidia Larizza Dipartimento di Scienze della Salute, Università degli Studi di Milano, Milan, Italy. 2.
Opitz trigonocephaly syndrome presenting with sudden unexplained...
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Laura Travan Affiliated with Neonatal Intensive Care Unit, Institute for Maternal and Child Health Burlo Garofolo Email author , Vanna Pecile Affiliated with ...
Reports & Statements
Wikipedia: Синдром тригоноцефалии Опица — Википедия
Laura Travan, Vanna Pecile, Mariacristina Fertz, Antonella Fabretto, Pierpaolo Brovedani, Sergio Demarini and John M Opitz ...
Chromosome instability and nibrin protein variants in NBS...
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Article. European Journal of Human Genetics (2003) 11, 297–303. doi: sj.ejhg Chromosome instability and nibrin protein variants in NBS heterozygotes. Caterina Tanzarella, Antonio Antoccia, Emanuela Spadoni, Alessandra di Masi, Vanna Pecile, Eliana Demori, Raymonda Varon, Gian Luigi Marseglia, ...
Excess of runs of homozygosity is associated with severe Nature
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Ilaria Gandin MSc,,; Flavio Faletra MD,,; Francesca Faletra MSc,,; Massimo Carella PhD,,; Vanna Pecile MSc,,; Giovanni B. Ferrero MD, PhD,, ...
Miscellaneous
Vanna Pecile | LinkedIn
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View Vanna Pecile's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Vanna Pecile discover inside ...
L'uso di SNP- array in diagnosi prenatale. Vanna Pecile IRCCS Burlo...
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L'uso di SNP- array in diagnosi prenatale Vanna Pecile IRCCS Burlo Garofolo Trieste Il cariotipo è in grado di evidenziare anomalie cromosomiche nel 8 35% di ...
Dott.ssa Vanna Pecile | IRCCS materno infantile Burlo Garofolo
www.burlo.trieste.it
Dott.ssa Vanna Pecile; Dott.ssa Vanna Pecile. Direttore f.f. Genetica Medica. Curriculum: pecilevanna.pdf. Email: Amministrazione Trasparente. Mappa veloce . Chi …
Vanna Pecile – Network — Italian Ministry of Health
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Vanna Pecile. IRCCS pediatrico Burlo Garofolo. .it Citations; 14 h-Index … Overview · Fingerprint · Network · Research Output (73) · Similar Profiles (32); NaNMore ...
Aplastic Anemia: Pecile, Vanna - Expertscape.com
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Vanna Pecile has special expertise in Anemia, Aplastic
Vanna Pecile
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Vanna Pecile. Details · Publications ... Flavio Faletra, Raffaella Devescovi, Vanna Pecile, Antonella Fabretto, more · Journal of Applied Genetics 52 ,
Vanna Pecile — Italian Ministry of Health
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Fingerprint Fingerprint is based on mining the text of the persons scientific documents to create an index of weighted terms, which defines the key subjects of each ...
Altmetric – 19p13 microduplications encompassing NFIX are ...
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... Colina McKeown, Gemma Poke, Kate Robertshaw, Eve Fifield, Antonella Fabretto, Vanna Pecile, Paolo Gasparini, Marco Carrozzi, Didier Lacombe, Benoît ...
AISIWH – Pubblicazioni Varie
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2008 WHS AJMG. MARCELLA ZOLLINO, MARINA MURDOLO, GIUSEPPE MARANGI, VANNA PECILE, CINZIA GALASSO, LAURA MAZZANTI, AND GIOVANNI NERI ...
CCAF - Appuntamenti marzo aprile 2014
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ore 20:30. Conferenza. GENETICA UMANA Nuove frontiere e nuove sfide. PIEGHEVOLE · LOCANDINA. Dott.ssa Vanna Pecile. Laboratorio Genetica Medica
Fragile X syndrome, mental retardation and macroorchidism | antonio...
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Fragile X syndrome, mental retardation and macroorchidism. Serena Vatta,; Ileana Cigui,; Eliana Demori,; Marcello Morgutti,; Vanna Pecile,; Daniela Gambel Benussi ...
Altmetric – A multi-method approach to the molecular diagnosis of...
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... Annalisa Calcagno, Mohamad Maghnie, Maria Teresa Divizia, Daniela Melis, Emanuela Manfredini, Giovanni Battista Ferrero, Vanna Pecile, ...
CTNND2 deletion and intellectual disability - INFONA
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Vanna Pecile. Institute for Maternal and Child Health — IRCCS “Burlo Garofolo”, Trieste, Italy. see all. Keywords. CTNND2 Deletion Intellectual Disability CNV.
De novo unbalanced translocations have a complex history/aetiology ...
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... Mana M. Mehrjouy, Aldesia Provenzano, Debora Vergani, Vanna Pecile, Francesca Novara, Paolo Reho, Marilena Carmela Di Giacomo, Giancarlo Discepoli, ...
Identification of point mutations and large intragenic deletions in...
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... Vanna Pecile, Angela D'Eustacchio, Enrico Cappelli, Paola Corti, Nicoletta Marra, Ugo Ramenghi, Marta Pillon, Piero Farruggia, Carlo Dufour, Alberto ...
Clinical and Molecular Cytogenetic Characterisation of Children with ...
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Sara Bertok / Mojca Žerjav Tanšek / Primož Kotnik / Tadej Battelino / Marija Volk / Vanna Pecile / Lisa Cleva / Paolo Gasparini / Jernej Kovač / Tinka Hovnik.
Cytogenetic and molecular evaluation of 241 small supernumerary...
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Breakthrough research or false findings? New review of: Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: Cooperative study...
FismeLab – Delegati regionali SIGUwww.fismelab.org/chi-siamo/delegati-regionali-sigu/
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Calabria, \. Campania, Gioacchino Scarano. . Emilia Romagna, Alberto Sensi. . Friuli Venezia Giulia, Vanna Pecile.
Opitz trigonocephaly syndrome presenting with sudden unexplained...
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Opitz trigonocephaly syndrome presenting with sudden unexplained death in the operating room: a case report. Laura Travan, Vanna Pecile, Mariacristina Fertz ...
Congresso Nazionale SIGU - PDF Free Download
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... COMITATO SCIENTIFICO Giorgio Casari - Coordinatore Francesca Forzano Giovanni Malerba Maria Giuseppina Miano Vanna Pecile Corrado Romano Silvia ...
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