TUCCI, ARIANNA
 Distribuzione geografica
Continente #
NA - Nord America 196
EU - Europa 57
AS - Asia 17
AF - Africa 3
SA - Sud America 2
Totale 275
Nazione #
US - Stati Uniti d'America 193
IT - Italia 32
DE - Germania 15
CN - Cina 13
FR - Francia 5
CA - Canada 3
ZA - Sudafrica 3
AE - Emirati Arabi Uniti 2
CL - Cile 2
GB - Regno Unito 2
IE - Irlanda 1
KR - Corea 1
LT - Lituania 1
TW - Taiwan 1
UA - Ucraina 1
Totale 275
Città #
Fairfield 44
Milan 32
Ashburn 16
Seattle 15
Woodbridge 15
Buffalo 12
Beijing 9
Cambridge 9
Santa Cruz 8
Wilmington 7
Ann Arbor 6
Houston 5
Clearwater 3
Muizenberg 3
Las Vegas 2
Mountain View 2
Nürnberg 2
Ottawa 2
Phoenix 2
Wuhan 2
Alexandria 1
Arkadelphia 1
Berlin 1
Boardman 1
Chicago 1
Columbus 1
Costa Mesa 1
Crugers 1
Dublin 1
Hamilton 1
Leeds 1
Los Angeles 1
Palo Alto 1
Provo 1
Riva 1
San Diego 1
Scottsdale 1
Southend 1
Taipei 1
University Park 1
Totale 216
Nome #
MIR137 is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletions, file dfa8b998-3bfe-748b-e053-3a05fe0a3a96 140
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz Syndrome, file dfa8b996-07f2-748b-e053-3a05fe0a3a96 125
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth, file dfa8b999-31b7-748b-e053-3a05fe0a3a96 8
16p13 microduplication without CREBBP involvement : moving toward a phenotype delineation, file dfa8b998-7e25-748b-e053-3a05fe0a3a96 4
16p13 microduplication without CREBBP involvement : moving toward a phenotype delineation, file dfa8b997-f928-748b-e053-3a05fe0a3a96 3
7p22.1 microduplication syndrome : refinement of the critical region, file dfa8b997-fe7a-748b-e053-3a05fe0a3a96 3
7p22.1 microduplication syndrome : refinement of the critical region, file dfa8b998-be98-748b-e053-3a05fe0a3a96 3
The absence that makes the difference: choroidal abnormalities in Legius syndrome, file dfa8b99a-932e-748b-e053-3a05fe0a3a96 2
New Insights into Kleefstra Syndrome : Report of Two Novel Cases with Previously Unreported Features and Literature Review, file dfa8b99d-c5ce-748b-e053-3a05fe0a3a96 2
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? : A case report and review of 62 cases, file dfa8b997-f292-748b-e053-3a05fe0a3a96 1
Totale 291
Categoria #
all - tutte 532
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 532


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201913 0 0 0 0 0 0 0 0 0 0 8 5
2019/202084 3 3 5 18 8 9 6 10 12 3 4 3
2020/202150 3 3 3 2 8 3 11 3 5 3 4 2
2021/202247 2 3 3 3 5 0 6 2 3 2 12 6
2022/202328 0 1 12 7 1 4 0 0 0 0 3 0
2023/202419 0 1 2 0 1 4 2 2 4 2 1 0
Totale 291