MINOTTI, CHIARA
 Distribuzione geografica
Continente #
AS - Asia 107
NA - Nord America 64
EU - Europa 59
SA - Sud America 27
AF - Africa 1
Totale 258
Nazione #
US - Stati Uniti d'America 61
SG - Singapore 57
IT - Italia 26
CN - Cina 20
BR - Brasile 19
HK - Hong Kong 15
NL - Olanda 7
VN - Vietnam 7
DE - Germania 5
GB - Regno Unito 5
VE - Venezuela 4
AT - Austria 3
FR - Francia 3
RU - Federazione Russa 3
AR - Argentina 2
FI - Finlandia 2
ID - Indonesia 2
MX - Messico 2
SE - Svezia 2
TR - Turchia 2
AE - Emirati Arabi Uniti 1
BD - Bangladesh 1
BG - Bulgaria 1
CA - Canada 1
CO - Colombia 1
IN - India 1
LT - Lituania 1
NP - Nepal 1
PL - Polonia 1
PY - Paraguay 1
ZA - Sudafrica 1
Totale 258
Città #
Singapore 34
Hong Kong 15
Los Angeles 8
Beijing 7
Ashburn 6
Caracas 4
Ho Chi Minh City 4
Rome 4
Amsterdam 3
Milan 3
New York 3
Ankara 2
Bergamo 2
Buffalo 2
Council Bluffs 2
Curitiba 2
Frankfurt am Main 2
Frascati 2
Helsinki 2
Mexico City 2
Nuremberg 2
Redondo Beach 2
Santa Clara 2
Stockholm 2
São Paulo 2
Zhengzhou 2
Asunción 1
Atlanta 1
Banfield 1
Belo Horizonte 1
Chennai 1
City of London 1
Da Nang 1
Dallas 1
Duque de Caxias 1
Greensboro 1
Guarulhos 1
Hangzhou 1
Hanoi 1
Houston 1
Jakarta 1
Johannesburg 1
Lombard 1
Londrina 1
Mogi das Cruzes 1
North Bergen 1
Nova Iguaçu 1
Orem 1
Pelotas 1
Philadelphia 1
Phoenix 1
Picos 1
Pittsburgh 1
Popayán 1
Poplar 1
Porto Alegre 1
Resistencia 1
Rio das Ostras 1
Rio de Janeiro 1
Seattle 1
Secaucus 1
Sofia 1
São Carlos 1
São Gabriel 1
São José 1
Tangerang 1
Teodoro Sampaio 1
Thái Nguyên 1
Toronto 1
Vienna 1
Warsaw 1
Weifang 1
Wuxi 1
Totale 168
Nome #
Genetic Variability of SOX10-Related Disorders within an Italian Family: Straddling the Line between Kallmann and Waardenburg Syndrome 70
Donor selection for allogeneic hematopoietic cell transplant in a patient with JAK2 V617F primary myelofibrosis and SH2B3/LNK germline variant 65
Case report: A new de novo 6q21q22.1 interstitial deletion case in a girl with cerebellar vermis hypoplasia and developmental delay and literature review 49
A Novel COL4A5 Pathogenic Variant Joins the Dots in a Family with a Synchronous Diagnosis of Alport Syndrome and Polycystic Kidney Disease 47
Co-Inheritance of Pathogenic Variants in PKD1 and PKD2 Genes Determined by Parental Segregation and De Novo Origin: A Case Report 45
Totale 276
Categoria #
all - tutte 1.107
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 1.107


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2024/2025145 0 55 7 3 6 14 20 4 10 6 15 5
2025/2026131 24 16 24 25 25 17 0 0 0 0 0 0
Totale 276