GENOVESI, MARIA LUCE
 Distribuzione geografica
Continente #
NA - Nord America 216
EU - Europa 182
AS - Asia 53
AF - Africa 3
OC - Oceania 1
Totale 455
Nazione #
US - Stati Uniti d'America 212
IT - Italia 132
SE - Svezia 12
IN - India 11
SG - Singapore 11
PK - Pakistan 9
FR - Francia 8
CH - Svizzera 7
CN - Cina 7
DE - Germania 6
KR - Corea 6
CA - Canada 4
IE - Irlanda 4
FI - Finlandia 3
IR - Iran 3
TR - Turchia 3
GR - Grecia 2
MA - Marocco 2
AU - Australia 1
BG - Bulgaria 1
ES - Italia 1
GB - Regno Unito 1
HK - Hong Kong 1
KG - Kirghizistan 1
NL - Olanda 1
NO - Norvegia 1
RO - Romania 1
RS - Serbia 1
TG - Togo 1
UA - Ucraina 1
VN - Vietnam 1
Totale 455
Città #
Rome 32
Fairfield 28
Ashburn 27
Chandler 13
Woodbridge 13
Houston 12
Cambridge 10
Seattle 9
Wilmington 8
Cagliari 7
Princeton 7
Islamabad 6
Ann Arbor 5
Boston 5
San Diego 5
San Paolo di Civitate 5
Dublin 4
Pully 4
Singapore 4
Ankara 3
Beijing 3
Boardman 3
Bremen 3
Dearborn 3
Kohat 3
Lawrence 3
Palermo 3
Plano 3
San Mateo 3
Toronto 3
Washington 3
Absecon 2
Athens 2
Bronx 2
Corona 2
Durham 2
Milan 2
New York 2
Norwalk 2
Padova 2
Pavia 2
Rabat 2
Redwood City 2
Reggio Emilia 2
Seongnam 2
Seoul 2
Albano Laziale 1
Arenys De Munt 1
Babraham 1
Berlin 1
Bishkek 1
Bologna 1
Bühl 1
Cori 1
Delft 1
Formello 1
Fucecchio 1
Galdo 1
Hamburg 1
Hanoi 1
Hefei 1
Helsinki 1
Hobart 1
Hong Kong 1
Kunming 1
Lomé 1
Los Angeles 1
Mentana 1
Millbury 1
Nanchang 1
Naples 1
Ottawa 1
Penne 1
Perugia 1
Phoenix 1
Préverenges 1
Ramacca 1
Sofia 1
Tehran 1
Torino 1
Viterbo 1
Yuncheng 1
Totale 306
Nome #
Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies 115
Next generation sequencing approaches in rare diseases: the study of four different families 89
GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlations 75
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritance 73
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation. 69
Fanconi anaemia, chromosome instability, DNA replication and fragile sites 68
Totale 489
Categoria #
all - tutte 1.223
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 1.223


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202078 0 0 0 3 9 9 20 9 9 5 3 11
2020/202189 5 5 6 2 7 5 0 15 14 12 18 0
2021/202291 4 4 14 4 10 7 1 8 4 4 15 16
2022/202367 13 14 10 4 6 4 2 4 8 1 1 0
2023/202491 1 7 9 7 11 10 3 9 3 11 16 4
2024/20258 2 4 2 0 0 0 0 0 0 0 0 0
Totale 489