TUCCI, ARIANNA
 Distribuzione geografica
Continente #
NA - Nord America 362
EU - Europa 310
AS - Asia 126
Continente sconosciuto - Info sul continente non disponibili 2
SA - Sud America 2
OC - Oceania 1
Totale 803
Nazione #
US - Stati Uniti d'America 346
GB - Regno Unito 138
CN - Cina 88
SE - Svezia 56
IT - Italia 32
CA - Canada 16
BE - Belgio 15
DE - Germania 15
IN - India 15
FI - Finlandia 11
IE - Irlanda 11
DK - Danimarca 9
SG - Singapore 7
FR - Francia 6
UA - Ucraina 6
HK - Hong Kong 5
ID - Indonesia 4
RO - Romania 3
BG - Bulgaria 2
BR - Brasile 2
KR - Corea 2
NL - Olanda 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AU - Australia 1
ES - Italia 1
EU - Europa 1
IQ - Iraq 1
IR - Iran 1
LT - Lituania 1
MY - Malesia 1
RS - Serbia 1
RU - Federazione Russa 1
TW - Taiwan 1
UZ - Uzbekistan 1
Totale 803
Città #
Southend 129
Chandler 65
Ann Arbor 52
Fairfield 42
Ashburn 24
Milan 21
Seattle 17
Princeton 16
Wilmington 16
Woodbridge 16
Cambridge 14
Toronto 14
Brussels 13
Guangzhou 12
Nanjing 12
Dublin 11
Dearborn 10
Beijing 8
Jinan 8
Hangzhou 7
Helsinki 7
Bengaluru 6
Des Moines 6
Phoenix 5
Boardman 4
Hong Kong 4
Houston 4
Mumbai 4
Shenyang 4
Haikou 3
Nanchang 3
Ningbo 3
Norwalk 3
Redwood City 3
Tianjin 3
Changsha 2
Edinburgh 2
Eschweiler 2
Hanover 2
London 2
Ottawa 2
Rome 2
Sofia 2
São Paulo 2
Taiyuan 2
Taizhou 2
Waanrode 2
Zhengzhou 2
Alexandria 1
Belgrade 1
Berlin 1
Bühl 1
Central District 1
Changchun 1
Chatsworth 1
Fremont 1
Jiaxing 1
Kaunas 1
Korbach 1
Kuala Lumpur 1
Lessolo 1
North Bergen 1
Redmond 1
San Diego 1
San Francisco 1
Seano 1
Shanghai 1
Shenzhen 1
Singapore 1
Taipei 1
Wenzhou 1
Ürümqi 1
Totale 619
Nome #
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth 145
MIR137 is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletions 138
7p22.1 microduplication syndrome : refinement of the critical region 130
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz Syndrome 120
16p13 microduplication without CREBBP involvement : moving toward a phenotype delineation 103
New Insights into Kleefstra Syndrome : Report of Two Novel Cases with Previously Unreported Features and Literature Review 91
The absence that makes the difference: choroidal abnormalities in Legius syndrome 82
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? : A case report and review of 62 cases 56
Totale 865
Categoria #
all - tutte 2.169
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 2.169


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201925 0 0 0 0 0 0 0 0 0 0 7 18
2019/2020165 17 5 2 23 9 16 14 10 36 22 3 8
2020/2021131 7 7 17 3 11 4 23 18 7 9 17 8
2021/2022125 15 8 8 5 2 6 3 3 24 11 8 32
2022/2023165 23 22 21 20 15 31 2 12 14 2 2 1
2023/202463 1 11 11 5 21 4 1 4 3 1 1 0
Totale 865