MORGUTTI, MARCELLO
 Distribuzione geografica
Continente #
NA - Nord America 586
EU - Europa 249
AS - Asia 71
AF - Africa 4
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 913
Nazione #
US - Stati Uniti d'America 586
PL - Polonia 100
SE - Svezia 50
CN - Cina 31
IT - Italia 29
HK - Hong Kong 25
BE - Belgio 16
UA - Ucraina 15
FI - Finlandia 9
TR - Turchia 9
IE - Irlanda 8
BG - Bulgaria 6
DE - Germania 6
GB - Regno Unito 3
SN - Senegal 3
AU - Australia 2
FR - Francia 2
NL - Olanda 2
VN - Vietnam 2
AT - Austria 1
BN - Brunei Darussalam 1
CH - Svizzera 1
ES - Italia 1
EU - Europa 1
IL - Israele 1
KR - Corea 1
SG - Singapore 1
ZA - Sudafrica 1
Totale 913
Città #
Warsaw 100
Fairfield 83
Ann Arbor 76
Woodbridge 73
Houston 54
Chandler 51
Ashburn 44
Seattle 35
Wilmington 32
Cambridge 27
Hong Kong 24
Jacksonville 20
Brussels 16
Princeton 14
Trieste 11
Izmir 9
Dearborn 8
Dublin 8
San Diego 6
Sofia 6
Beijing 5
Boardman 4
Helsinki 4
Dakar 3
Guangzhou 3
Norwalk 3
Amsterdam 2
Bremen 2
Changsha 2
Des Moines 2
Dong Ket 2
Fuzhou 2
Haikou 2
Hefei 2
Mestre 2
Milan 2
Padova 2
Allentown 1
Andover 1
Bandar Seri Begawan 1
Barletta 1
Bern 1
Central 1
Columbus 1
Dongguan 1
Gava 1
Hangzhou 1
Huzhou 1
Indiana 1
Jinan 1
Johannesburg 1
Krefeld 1
Kunming 1
Los Angeles 1
Melbourne 1
Nanchang 1
Paris 1
Phoenix 1
Pignone 1
Seoul 1
Shanghai 1
Shenyang 1
Siena 1
Tel Aviv 1
Tianjin 1
Trento 1
Vienna 1
Totale 771
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 257
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 157
Short Communication Novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients 138
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients 134
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss 115
Five new OTOF gene mutations and auditory neuropathy 92
Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis 51
Totale 944
Categoria #
all - tutte 2.275
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 2.275


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201974 0 0 0 0 0 0 0 0 0 17 37 20
2019/2020244 14 10 14 40 18 26 25 20 35 13 16 13
2020/2021194 18 26 15 15 21 8 23 8 25 12 14 9
2021/2022101 12 3 6 4 4 8 4 6 10 12 6 26
2022/2023161 16 16 10 25 17 28 0 15 18 2 10 4
2023/202477 4 7 3 8 5 7 19 19 1 4 0 0
Totale 944