FABRETTO, ANTONELLA
 Distribuzione geografica
Continente #
NA - Nord America 201
EU - Europa 50
AS - Asia 24
SA - Sud America 3
AF - Africa 2
Totale 280
Nazione #
US - Stati Uniti d'America 199
IT - Italia 27
CN - Cina 14
FR - Francia 6
GB - Regno Unito 6
DE - Germania 4
JP - Giappone 4
CA - Canada 2
CL - Cile 2
DK - Danimarca 2
ES - Italia 2
HK - Hong Kong 2
PL - Polonia 2
TR - Turchia 2
VN - Vietnam 2
BE - Belgio 1
BR - Brasile 1
SN - Senegal 1
ZA - Sudafrica 1
Totale 280
Città #
Fairfield 28
Ashburn 25
Cambridge 16
Wilmington 15
Beijing 12
Trieste 12
Woodbridge 12
Seattle 11
Buffalo 6
Cincinnati 6
Santa Cruz 6
Altrincham 5
Ann Arbor 5
Madison 5
Syracuse 5
Boardman 4
Houston 4
Las Vegas 4
Milan 4
Aurora 2
Austin 2
Bonn 2
Carugate 2
Copenhagen 2
Dong Ket 2
Mountain View 2
Raleigh 2
San Diego 2
San Jose 2
Tokyo 2
Valencia 2
Warsaw 2
Aksaray 1
Alexandria 1
Antwerp 1
Bremen 1
Central 1
Chicago 1
Dakar 1
Dallas 1
Denver 1
Ehime 1
Falls Church 1
Frankfurt am Main 1
Friendswood 1
Grenoble 1
Hangzhou 1
Hong Kong 1
Izmir 1
Jaboatao dos Guararapes 1
Lake Forest 1
Muizenberg 1
New York 1
Ottawa 1
Pasadena 1
Phoenix 1
Reggio Nell'emilia 1
Rochester 1
San Francisco 1
Santiago 1
Sondrio 1
South Bend 1
Victoria 1
Yellow Springs 1
Totale 243
Nome #
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders, file e2913fdc-d4fc-f688-e053-3705fe0a67e0 178
A new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome, file e2913fdf-8a4e-f688-e053-3705fe0a67e0 48
Two cases of Noonan syndrome with severe respiratory and gastroenteral involvement and the SOS1 mutation F623I, file e2913fdc-8583-f688-e053-3705fe0a67e0 17
Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12, file e2913fdc-94ef-f688-e053-3705fe0a67e0 12
A Validated HPLC-Diode Array Detection Method for Therapeutic Drug Monitoring of Thiopurines in Pediatric Patients: From Bench to Bedside, file 72024c06-f5bb-488e-9044-c6220f805314 10
Prevalence and characteristics of thelarche variant, file 4f4cdff3-2e7c-48ab-9607-36401240f36b 6
De novo 6.9Mb interstitial deletion on chromosome 4q31.1-q32.1 in a girl with severe speech delay and dysmorphic features, file e2913fdc-857a-f688-e053-3705fe0a67e0 6
A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation, file e2913fdc-c4be-f688-e053-3705fe0a67e0 6
A new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome, file e2913fde-0e60-f688-e053-3705fe0a67e0 5
19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference, file e2913fdc-415e-f688-e053-3705fe0a67e0 2
Alagille syndrome: A new missense mutation detected by whole-exome sequencing in a case previously found to be negative by DHPLC and MLPA, file e2913fdc-96ba-f688-e053-3705fe0a67e0 1
Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures, file e2913fdc-9f7b-f688-e053-3705fe0a67e0 1
A new case of duplication of the MDS region identified by high-density SNP arrays and a review of the literature, file e2913fdc-c4ba-f688-e053-3705fe0a67e0 1
Totale 293
Categoria #
all - tutte 592
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 592


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202076 4 7 10 14 6 4 5 6 9 5 4 2
2020/202154 3 4 5 5 4 6 2 12 1 6 2 4
2021/202233 1 5 1 3 1 1 2 2 6 1 7 3
2022/202390 4 1 12 8 11 5 16 5 6 14 8 0
2023/202438 2 4 4 2 2 5 6 12 0 1 0 0
Totale 293