RIGON, CHIARA
 Distribuzione geografica
Continente #
NA - Nord America 309
EU - Europa 168
AS - Asia 26
Continente sconosciuto - Info sul continente non disponibili 1
Totale 504
Nazione #
US - Stati Uniti d'America 309
IT - Italia 127
DE - Germania 13
CN - Cina 12
SG - Singapore 12
FI - Finlandia 7
FR - Francia 6
SE - Svezia 5
GB - Regno Unito 3
UA - Ucraina 3
DK - Danimarca 1
EU - Europa 1
HU - Ungheria 1
IE - Irlanda 1
IL - Israele 1
IN - India 1
RU - Federazione Russa 1
Totale 504
Città #
Houston 41
Fairfield 38
Chandler 37
Ashburn 22
Seattle 21
Woodbridge 15
Wilmington 14
Cambridge 13
Ann Arbor 12
Naples 12
Jacksonville 11
Singapore 10
Milan 8
Redmond 7
Bari 6
Cagliari 6
Princeton 6
Quinto di Treviso 6
Beijing 5
Ravenna 5
Boardman 4
Giovinazzo 4
Helsinki 4
Medford 4
Padova 4
Rome 4
San Diego 4
Turin 4
Venice 4
Monreale 3
New York 3
Adelfia 2
Bologna 2
Canegrate 2
Capitol Heights 2
Cecina 2
Cormano 2
Des Moines 2
Faggiano 2
Florence 2
Fregona 2
Fremont 2
Limbiate 2
Longarone 2
Marano di Napoli 2
Napoli 2
Nardò 2
Noicattaro 2
Ogden 2
Paris 2
Parma 2
San Giovanni in Persiceto 2
Siena 2
Usmate Velate 2
Verona 2
Alpharetta 1
Anguillara 1
Atlanta 1
Battipaglia 1
Bayonne 1
Bergamo 1
Budapest 1
Camponogara 1
Cava 1
Changsha 1
Copenhagen 1
Dongguan 1
Dublin 1
Edinburgh 1
Kirkland 1
Lappeenranta 1
London 1
Mira 1
Mumbai 1
Nanjing 1
Norwalk 1
Nürnberg 1
Rieti 1
Rockville 1
Saint Petersburg 1
San Casciano in Val di Pesa 1
Sassari 1
Seriate 1
Shenyang 1
Stockholm 1
Tappahannock 1
Tel Aviv 1
Washington 1
Totale 418
Nome #
Caratterizzazione molecolare mediante array-CGH e origine parentale di anomalie cromosomiche strutturali in pazienti con ritardo mentale/psicomotorio/autismo e/o anomalie comportamentali 174
A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus 110
Association study of AMH and AMHRII polymorphisms with unexplained infertility. 97
Auditory Outcome after Cochlear Implantation in Children with DFNB7/11 Caused by Pathogenic Variants in TMC1 Gene 68
DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature 39
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome 9
Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature 9
From clinical to molecular diagnosis: relevance of diagnostic strategy in two cases of branchio-oto-renal syndrome - case report 6
Totale 512
Categoria #
all - tutte 2.469
article - articoli 1.855
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.324


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202037 0 0 1 4 5 6 4 5 5 3 3 1
2020/202166 3 1 1 5 3 1 19 6 8 5 5 9
2021/202261 6 3 3 0 2 7 6 3 7 9 6 9
2022/2023111 11 2 3 15 14 13 0 13 19 5 15 1
2023/2024156 5 6 16 15 8 17 19 17 8 7 17 21
2024/202513 10 3 0 0 0 0 0 0 0 0 0 0
Totale 512