FINI, Sergio
 Distribuzione geografica
Continente #
NA - Nord America 783
EU - Europa 183
AS - Asia 74
AF - Africa 4
SA - Sud America 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.047
Nazione #
US - Stati Uniti d'America 781
IT - Italia 64
CN - Cina 59
UA - Ucraina 31
DE - Germania 29
GB - Regno Unito 26
SE - Svezia 13
TR - Turchia 8
FI - Finlandia 7
BE - Belgio 5
DZ - Algeria 4
SI - Slovenia 3
CA - Canada 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 1.047
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
Bremen 8
San Diego 8
Shanghai 8
Dearborn 7
Izmir 7
Boardman 6
Brussels 5
Bologna 4
Pisa 4
London 3
Mcallen 3
Munich 3
Padova 3
San Mateo 3
Algiers 2
Des Moines 2
Dong Ket 2
Falls Church 2
Guangzhou 2
Helsinki 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 817
Nome #
Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay 117
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome 112
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies 111
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders. 111
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 109
Transcriptional behavior of DMD gene duplications in DMD/BMD males 105
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 99
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 90
A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the Literature 85
DMD gene molecular genetic characterization in Eastern Europe and non European countries 74
Workload measurement for molecular genetics laboratory: A survey study 55
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotype 3
Totale 1.071
Categoria #
all - tutte 4.671
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 4.671


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201979 0 0 0 0 0 0 0 0 0 0 37 42
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
2023/202479 8 12 4 0 5 30 4 7 1 2 6 0
Totale 1.071