MORGUTTI, MARCELLO
 Distribuzione geografica
Continente #
NA - Nord America 181
EU - Europa 107
AS - Asia 58
OC - Oceania 5
AF - Africa 3
SA - Sud America 3
Totale 357
Nazione #
US - Stati Uniti d'America 177
IT - Italia 36
CN - Cina 31
CZ - Repubblica Ceca 15
NL - Olanda 13
UA - Ucraina 10
DE - Germania 8
IR - Iran 7
GB - Regno Unito 6
AU - Australia 5
IN - India 5
RU - Federazione Russa 5
CA - Canada 4
FR - Francia 4
CL - Cile 3
KR - Corea 3
BE - Belgio 2
HK - Hong Kong 2
PL - Polonia 2
SA - Arabia Saudita 2
SG - Singapore 2
SN - Senegal 2
TR - Turchia 2
VN - Vietnam 2
ES - Italia 1
IS - Islanda 1
LB - Libano 1
LU - Lussemburgo 1
NO - Norvegia 1
SE - Svezia 1
SI - Slovenia 1
TW - Taiwan 1
UG - Uganda 1
Totale 357
Città #
Ashburn 22
Fairfield 20
Woodbridge 14
Buffalo 13
Houston 11
Trieste 9
Pavia 8
Santa Cruz 8
Seattle 8
Shanghai 8
Wilmington 7
Beijing 6
Ann Arbor 4
Atlanta 4
Boardman 3
Cambridge 3
Guangzhou 3
Las Vegas 3
Los Angeles 3
Melbourne 3
Mountain View 3
Tucson 3
Boston 2
Campi Bisenzio 2
Chennai 2
Chicago 2
Dakar 2
Dong Ket 2
Dongguan 2
Frankfurt am Main 2
Hackney 2
Jeddah 2
Lexington 2
Rome 2
San Jose 2
Sasso Marconi 2
Sunnyvale 2
Turin 2
Warsaw 2
Allentown 1
Amsterdam 1
Antegnate 1
Ashton-under-Lyne 1
Asker 1
Barletta 1
Bengaluru 1
Bologna 1
Canberra 1
Central 1
Clearwater 1
Cologne 1
Council Bluffs 1
Crugers 1
Des Moines 1
Edirne 1
Garðabaer 1
Ghent 1
Göttingen 1
Halifax 1
Hangzhou 1
Harringay 1
Iowa City 1
Kampala 1
Kanata 1
Ljubljana 1
London 1
Milan 1
Moscow 1
Naples 1
New York 1
Ottawa 1
Palermo 1
Perth 1
Phoenix 1
Pune 1
Quarto d'Altino 1
Quartu Sant'Elena 1
Riva 1
Salt Lake City 1
Santiago 1
Sariyer 1
St Petersburg 1
Stockholm 1
Taipei 1
Taizhou 1
Tripoli 1
University Park 1
Valencia 1
Verrua Po 1
Wanchai 1
Winchester 1
Wuhan 1
Yellow Springs 1
Yerington 1
Totale 255
Nome #
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations, file e2913fdc-7082-f688-e053-3705fe0a67e0 218
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis, file e2913fdf-314d-f688-e053-3705fe0a67e0 79
Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis, file 9439b5a3-3765-4690-ac16-de875ae989ea 27
Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis, file abae329c-9886-4442-859a-3dd640692670 26
Five new OTOF gene mutations and auditory neuropathy, file e2913fdc-94fc-f688-e053-3705fe0a67e0 5
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis, file e2913fd9-a6b3-f688-e053-3705fe0a67e0 4
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss, file e2913fdc-f927-f688-e053-3705fe0a67e0 2
Totale 361
Categoria #
all - tutte 716
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 716


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201913 0 0 0 0 0 0 0 0 0 6 6 1
2019/202048 1 4 6 8 5 2 3 3 8 2 4 2
2020/202158 4 19 2 1 4 1 5 5 7 5 4 1
2021/202229 6 1 3 1 2 4 0 0 1 2 6 3
2022/202390 5 6 10 6 6 6 3 10 13 7 11 7
2023/2024121 14 15 21 8 16 14 7 8 2 16 0 0
Totale 361