FABRETTO, ANTONELLA
 Distribuzione geografica
Continente #
NA - Nord America 184
EU - Europa 34
AS - Asia 8
SA - Sud America 2
AF - Africa 1
Totale 229
Nazione #
US - Stati Uniti d'America 182
IT - Italia 21
GB - Regno Unito 5
JP - Giappone 4
CA - Canada 2
CL - Cile 2
DE - Germania 2
ES - Italia 2
PL - Polonia 2
VN - Vietnam 2
BE - Belgio 1
FR - Francia 1
HK - Hong Kong 1
TR - Turchia 1
ZA - Sudafrica 1
Totale 229
Città #
Fairfield 28
Ashburn 16
Cambridge 16
Wilmington 15
Woodbridge 12
Seattle 11
Fleming Island 10
Trieste 10
Cincinnati 6
Santa Cruz 6
Altrincham 5
Ann Arbor 5
Buffalo 5
Houston 4
Las Vegas 4
Milan 4
Boardman 3
Dong Ket 2
Mountain View 2
Raleigh 2
San Diego 2
San Jose 2
Tokyo 2
Valencia 2
Warsaw 2
Aksaray 1
Antwerp 1
Bremen 1
Central 1
Chicago 1
Dallas 1
Denver 1
Ehime 1
Falls Church 1
Frankfurt am Main 1
Friendswood 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 201
Nome #
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders, file e2913fdc-d4fc-f688-e053-3705fe0a67e0 170
A new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome, file e2913fdf-8a4e-f688-e053-3705fe0a67e0 27
Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12, file e2913fdc-94ef-f688-e053-3705fe0a67e0 12
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 7
Two cases of Noonan syndrome with severe respiratory and gastroenteral involvement and the SOS1 mutation F623I, file e2913fdc-8583-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
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 4
A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation, file e2913fdc-c4be-f688-e053-3705fe0a67e0 4
Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures, file e2913fdc-9f7b-f688-e053-3705fe0a67e0 3
19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference, file e2913fdc-415e-f688-e053-3705fe0a67e0 2
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 2
Totale 242
Categoria #
all - tutte 317
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 317


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20192 0020 00 00 0000
2019/202076 471014 64 56 9542
2020/202154 3455 46 212 1624
2021/202233 1513 11 22 6173
2022/202377 41128 115 2210 4000
Totale 242