FINI, Sergio
 Distribuzione geografica
Continente #
NA - Nord America 784
EU - Europa 186
AS - Asia 96
AF - Africa 4
SA - Sud America 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.073
Nazione #
US - Stati Uniti d'America 782
IT - Italia 65
CN - Cina 63
UA - Ucraina 31
DE - Germania 29
GB - Regno Unito 26
SG - Singapore 16
SE - Svezia 13
TR - Turchia 8
FI - Finlandia 7
BE - Belgio 5
DZ - Algeria 4
SI - Slovenia 3
CA - Canada 2
CZ - Repubblica Ceca 2
ID - Indonesia 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 1.073
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
Ferrara 16
Milan 12
Nanjing 12
Princeton 12
Shanghai 12
Singapore 11
Bremen 8
San Diego 8
Boardman 7
Dearborn 7
Izmir 7
Bologna 5
Brussels 5
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
Jakarta 2
Kunming 2
Los Angeles 2
Norwalk 2
Orange 2
Redwood City 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 838
Nome #
Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay 118
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies 115
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders. 114
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome 114
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 111
Transcriptional behavior of DMD gene duplications in DMD/BMD males 107
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 102
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 92
A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the Literature 87
DMD gene molecular genetic characterization in Eastern Europe and non European countries 75
Workload measurement for molecular genetics laboratory: A survey study 57
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotype 5
Totale 1.097
Categoria #
all - tutte 5.162
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 5.162


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020285 27 8 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
2024/20254 4 0 0 0 0 0 0 0 0 0 0 0
Totale 1.097