Carapelle, Marina
 Distribuzione geografica
Continente #
AS - Asia 89
NA - Nord America 87
EU - Europa 47
SA - Sud America 9
AF - Africa 1
Totale 233
Nazione #
US - Stati Uniti d'America 81
SG - Singapore 29
VN - Vietnam 19
IT - Italia 18
CN - Cina 17
DE - Germania 9
BR - Brasile 7
HK - Hong Kong 7
FR - Francia 6
FI - Finlandia 4
CA - Canada 3
IQ - Iraq 3
JP - Giappone 3
TW - Taiwan 3
AR - Argentina 2
GB - Regno Unito 2
IE - Irlanda 2
MX - Messico 2
NL - Olanda 2
PK - Pakistan 2
SE - Svezia 2
DZ - Algeria 1
ID - Indonesia 1
JM - Giamaica 1
KR - Corea 1
LB - Libano 1
LK - Sri Lanka 1
PL - Polonia 1
TR - Turchia 1
UA - Ucraina 1
UZ - Uzbekistan 1
Totale 233
Città #
Singapore 15
San Jose 12
Ashburn 10
Rome 10
Ho Chi Minh City 8
New York 7
Hanoi 6
Santa Clara 6
Council Bluffs 4
Lappeenranta 4
Los Angeles 4
Frankfurt am Main 3
Hefei 3
Lauterbourg 3
Munich 3
St Louis 3
São Paulo 3
Taipei 3
Tokyo 3
Chicago 2
Dublin 2
Hong Kong 2
Milan 2
Modena 2
Montreal 2
Portsmouth 2
The Dalles 2
Tianjin 2
Ankara 1
Atlanta 1
Baghdad 1
Basra 1
Beijing 1
Boston 1
Buffalo 1
Buon Ma Thuot 1
Can Tho 1
Charlotte 1
Chascomús 1
Colombo 1
Concord 1
Constantine 1
Curitiba 1
Denver 1
East Peoria 1
Faisalabad 1
Falkenstein 1
Foshan 1
Guadalupe 1
Haiphong 1
Hollywood 1
Houston 1
Jakarta 1
Juazeiro 1
Karachi 1
Kent 1
Kingston 1
Kowloon Tong 1
Lenoir 1
Lexington 1
Lviv 1
Matriz de Camaragibe 1
Mexico City 1
Morón 1
Mosul 1
Naaldwijk 1
Natal 1
North Bergen 1
Nuremberg 1
Paris 1
Paterson 1
Seattle 1
Seoul 1
Shanghai 1
Shijiazhuang 1
Stockholm 1
Tashkent 1
Tseung Kwan O 1
Waldshut-Tiengen 1
Warsaw 1
Washington 1
Ấp Tháp Mười 1
Totale 182
Nome #
Linear Diagnostic Procedure Elicited by Clinical Genetics and Validated by mRNA Analysis in Neuronal Ceroid Lipofuscinosis 7 Associated with a Novel Non-Canonical Splice Site Variant in MFSD8 140
Clinical-Genetic Approach to Conditions with Macrocephaly and ASD/Behaviour Abnormalities: Variants in PTEN and PPP2R5D Are the Most Recurrent Gene Mutations in a Patient-Oriented Diagnostic Strategy 55
The same genomic variants in the first three exons of KANSL1 can be either benign or causative of Koolen-de Vries syndrome: Definition of a validation procedure 41
Totale 236
Categoria #
all - tutte 1.284
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 1.284


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/20234 0 0 0 0 0 0 0 0 0 3 1 0
2023/202414 1 3 1 1 3 2 1 0 0 0 0 2
2024/202534 0 1 1 0 3 2 2 1 3 4 7 10
2025/2026184 9 2 4 16 24 25 51 22 15 16 0 0
Totale 236