FINI, Sergio
 Distribuzione geografica
Continente #
NA - Nord America 803
EU - Europa 186
AS - Asia 106
AF - Africa 4
SA - Sud America 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.102
Nazione #
US - Stati Uniti d'America 801
IT - Italia 65
CN - Cina 64
UA - Ucraina 31
DE - Germania 29
GB - Regno Unito 26
SG - Singapore 23
SE - Svezia 13
TR - Turchia 8
FI - Finlandia 7
BE - Belgio 5
DZ - Algeria 4
ID - Indonesia 4
SI - Slovenia 3
CA - Canada 2
CZ - Repubblica Ceca 2
NL - Olanda 2
VN - Vietnam 2
AE - Emirati Arabi Uniti 1
BD - Bangladesh 1
BR - Brasile 1
CL - Cile 1
ES - Italia 1
EU - Europa 1
FR - Francia 1
HU - Ungheria 1
IN - India 1
IR - Iran 1
SA - Arabia Saudita 1
Totale 1.102
Città #
Fairfield 123
Chandler 82
Woodbridge 82
Ashburn 57
Houston 55
Ann Arbor 49
Seattle 48
Cambridge 38
Jacksonville 33
Wilmington 30
Beijing 24
New York 22
Singapore 18
Ferrara 16
Milan 12
Nanjing 12
Princeton 12
Shanghai 12
Los Angeles 11
Bremen 8
San Diego 8
Boardman 7
Dearborn 7
Izmir 7
Bologna 5
Brussels 5
Jakarta 4
Pisa 4
London 3
Mcallen 3
Munich 3
Padova 3
San Mateo 3
Algiers 2
Brno 2
Des Moines 2
Dong Ket 2
Falls Church 2
Guangzhou 2
Helsinki 2
Kunming 2
Norwalk 2
Orange 2
Redwood City 2
Santa Clara 2
Shenyang 2
Tianjin 2
Trento 2
Zhengzhou 2
Argenta 1
Augusta 1
Budapest 1
Changsha 1
Dubai 1
Hebei 1
Jiaxing 1
Lowell 1
Modena 1
Montreal 1
Montréal 1
Mountain View 1
Nanchang 1
Ningbo 1
Philadelphia 1
Riyadh 1
São Paulo 1
Tappahannock 1
Washington 1
Yellow Springs 1
Totale 858
Nome #
Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay 120
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies 118
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome 117
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders. 115
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 112
Transcriptional behavior of DMD gene duplications in DMD/BMD males 110
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 106
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 95
A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the Literature 90
DMD gene molecular genetic characterization in Eastern Europe and non European countries 76
Workload measurement for molecular genetics laboratory: A survey study 61
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotype 6
Totale 1.126
Categoria #
all - tutte 5.851
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 5.851


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020250 0 0 8 44 22 36 34 31 30 29 11 5
2020/2021157 14 8 14 9 16 17 6 16 3 18 23 13
2021/2022157 8 6 3 4 21 10 8 13 12 14 10 48
2022/2023183 17 24 5 24 29 18 13 14 33 1 3 2
2023/2024101 8 12 4 0 5 30 4 7 1 2 6 22
2024/202533 4 11 18 0 0 0 0 0 0 0 0 0
Totale 1.126