ZUFFARDI, ORSETTA
 Distribuzione geografica
Continente #
NA - Nord America 135
AS - Asia 105
EU - Europa 88
SA - Sud America 16
AF - Africa 15
Totale 359
Nazione #
US - Stati Uniti d'America 133
SG - Singapore 62
IT - Italia 55
CN - Cina 29
IE - Irlanda 15
BR - Brasile 13
CI - Costa d'Avorio 8
KR - Corea 6
FR - Francia 4
GB - Regno Unito 4
IN - India 4
NG - Nigeria 4
CA - Canada 2
DE - Germania 2
FI - Finlandia 2
NL - Olanda 2
RU - Federazione Russa 2
AE - Emirati Arabi Uniti 1
AR - Argentina 1
CL - Cile 1
EG - Egitto 1
GR - Grecia 1
JP - Giappone 1
PK - Pakistan 1
SN - Senegal 1
UA - Ucraina 1
VE - Venezuela 1
VN - Vietnam 1
ZA - Sudafrica 1
Totale 359
Città #
Santa Clara 45
Dallas 34
Singapore 31
Hefei 18
Dublin 15
Civitanova Marche 12
Catania 11
Ashburn 10
Abidjan 8
Boardman 7
Messina 7
Chicago 6
Seoul 6
Palermo 5
Abuja 4
Beijing 4
Pune 3
Andover 2
Camberwell 2
Cambridge 2
Des Moines 2
Lappeenranta 2
Lawrence 2
Los Angeles 2
Milan 2
Nantes 2
Valenciennes 2
Washington 2
Alessandria 1
Amsterdam 1
Augusta 1
Berazategui 1
Cairo 1
Canoas 1
Canápolis 1
Chennai 1
Dakar 1
Denver 1
Esteio 1
Franca 1
Gunzenhausen 1
Hanoi 1
Houston 1
Hualpén 1
Itajaí 1
Johannesburg 1
La Villa del Rosario 1
Lahore 1
London 1
Macaé 1
Maceió 1
Monte Aprazível 1
Monte Carmelo 1
Montreal 1
New York 1
Newham 1
Nuremberg 1
Panambi 1
Poltava 1
Rome 1
Russell Springs 1
Santa Fe 1
Seattle 1
São Leopoldo 1
Urubici 1
Volta Redonda 1
Zhuhai 1
Totale 287
Nome #
Assigning single clinical features to their disease-locus in large deletions: the example of chromosome 1q23-25 deletion syndrome 98
Low-level complex mosaic with multiple cell lines affecting the 18q21.31q21.32 region in a patient with de novo 18q terminal deletion 70
The embryo battle against adverse genomes: Are de novo terminal deletions the rescue of unfavorable zygotic imbalances? 60
Targeted next-generation sequencing identifies the disruption of the SHANK3 and RYR2 genes in a patient carrying a de novo t(1;22)(q43;q13.3) associated with signs of Phelan-McDermid syndrome 51
The Italian XLMR bank: A clinical and molecular database 47
Erratum: The 2q23.1 microdeletion syndrome: Clinical and behavioural phenotype (European Journal of Human Genetics (2010) 18 (163-170) DOI: 10.1038/ejhg.2009.152) 41
Totale 367
Categoria #
all - tutte 1.352
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 1.352


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202112 0 0 0 0 0 0 2 7 3 0 0 0
2021/202227 0 2 0 0 2 0 2 0 0 1 0 20
2022/202338 4 0 0 0 2 11 0 8 8 0 1 4
2023/202435 0 0 5 2 1 13 1 1 0 3 4 5
2024/2025150 7 19 8 13 35 18 8 2 4 10 14 12
2025/2026105 24 22 43 16 0 0 0 0 0 0 0 0
Totale 367