ORZAN, FRANCESCA
 Distribuzione geografica
Continente #
EU - Europa 479
NA - Nord America 289
AS - Asia 109
SA - Sud America 6
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 885
Nazione #
US - Stati Uniti d'America 280
GB - Regno Unito 228
SE - Svezia 73
CN - Cina 51
IT - Italia 50
DE - Germania 38
UA - Ucraina 32
IN - India 20
TR - Turchia 17
KR - Corea 12
RU - Federazione Russa 12
IE - Irlanda 10
NL - Olanda 10
FI - Finlandia 9
CA - Canada 7
EU - Europa 7
CO - Colombia 6
HK - Hong Kong 6
FR - Francia 5
BE - Belgio 4
GR - Grecia 2
JP - Giappone 2
MX - Messico 2
NO - Norvegia 2
RS - Serbia 2
AU - Australia 1
ES - Italia 1
HU - Ungheria 1
ID - Indonesia 1
Totale 891
Città #
Southend 202
Chandler 40
Jacksonville 26
Wilmington 18
Princeton 16
Beijing 14
Seattle 14
Ann Arbor 13
Ashburn 13
Redmond 13
Woodbridge 13
Dearborn 12
Milan 12
Mountain View 12
Houston 11
Dublin 10
Nanjing 9
Serra 8
Andover 6
Bogotá 6
Hong Kong 6
Sakarya 6
Somerville 6
Boardman 5
Pisa 5
Toronto 5
Auburn Hills 4
Berlin 4
New York 4
San Diego 4
Zogno 4
Bengaluru 3
Bühl 3
Falls Church 3
Frankfurt am Main 3
Fuzhou 3
Helsinki 3
Phoenix 3
Shanghai 3
Verona 3
Waanrode 3
Zhengzhou 3
Arluno 2
Athens 2
Des Moines 2
Fairfield 2
Haikou 2
Hanover 2
Hebei 2
Jiaxing 2
Los Angeles 2
Offanengo 2
Roxbury 2
San Francisco 2
Taiyuan 2
Barzanò 1
Brussels 1
Budapest 1
Canary Wharf 1
Changchun 1
Changsha 1
Charlotte 1
Chilpancingo 1
Costa Mesa 1
Eitensheim 1
Frankfurt Am Main 1
Hamburg 1
Hefei 1
Jakarta 1
Jinan 1
Johanneshov 1
Lanzhou 1
London 1
Mexico 1
Minneapolis 1
Nanchang 1
Ningbo 1
Noginsk 1
Norwalk 1
Ottawa 1
Pune 1
Redwood City 1
Saint John's 1
Sevilla 1
Tappahannock 1
Washington 1
Wuppertal 1
Ürümqi 1
Totale 613
Nome #
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions 209
Uncommon Alu-mediated NF1 microdeletion with a breakpoint inside the NF1 gene 181
Genotype-phenotype correlation in patients with NF1 microdeletion syndrome : identification of candidate genes for mental retardation 149
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele 147
Evaluation of 1p36 markers and clinical outcome in a skull base chordoma study 141
Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis 113
Totale 940
Categoria #
all - tutte 1.765
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 1.765


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201927 0 0 0 0 0 0 0 0 0 1 13 13
2019/2020108 13 7 5 3 8 15 18 2 17 10 7 3
2020/2021134 12 8 15 0 8 5 7 6 17 8 42 6
2021/2022115 9 2 9 6 12 7 11 3 12 17 12 15
2022/2023111 21 18 9 11 15 21 0 5 11 0 0 0
2023/202443 2 6 6 2 15 6 0 3 2 1 0 0
Totale 940