FANTASIA, DONATELLA
 Distribuzione geografica
Continente #
NA - Nord America 416
EU - Europa 393
AS - Asia 247
SA - Sud America 3
AF - Africa 2
Totale 1.061
Nazione #
US - Stati Uniti d'America 416
CN - Cina 94
SG - Singapore 68
UA - Ucraina 64
IT - Italia 54
GB - Regno Unito 52
IE - Irlanda 52
SE - Svezia 48
DE - Germania 43
IN - India 41
TR - Turchia 35
FR - Francia 31
FI - Finlandia 22
RU - Federazione Russa 15
CZ - Repubblica Ceca 6
BE - Belgio 4
VN - Vietnam 4
BR - Brasile 2
IL - Israele 2
BD - Bangladesh 1
EC - Ecuador 1
IR - Iran 1
NL - Olanda 1
RO - Romania 1
SC - Seychelles 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 1.061
Città #
Chandler 102
Jacksonville 75
Dublin 52
Southend 46
Singapore 40
Princeton 27
Nanjing 24
Izmir 23
Dearborn 20
Beijing 17
Grafing 16
Cambridge 12
Ann Arbor 11
Boardman 11
Nanchang 11
Altamura 10
Wilmington 10
Ashburn 9
Chieti 9
Helsinki 9
Hebei 7
Shenyang 7
Tianjin 7
Brno 6
Kunming 6
Santa Clara 6
Los Angeles 5
Pescara 5
Woodbridge 5
Brussels 4
Dong Ket 4
New York 4
Grevenbroich 3
Hangzhou 3
Munich 3
Norwalk 3
Auburn Hills 2
Clifton 2
Düsseldorf 2
Espoo 2
Hefei 2
Jiaxing 2
Kfar Saba 2
Melendugno 2
Moscow 2
Ningbo 2
Teramo 2
Washington 2
Ürümqi 2
Ardabil 1
Augusta 1
Bologna 1
Bucharest 1
Changchun 1
Changsha 1
Cuenca 1
Edinburgh 1
Frankfurt am Main 1
Harbin 1
Isernia 1
Jinan 1
Johannesburg 1
Milan 1
Monmouth Junction 1
Mumbai 1
Orange 1
Roseto Degli Abruzzi 1
Sambuceto 1
San Francisco 1
Sangão 1
Stockholm 1
São Paulo 1
Taipei 1
Totale 662
Nome #
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 109
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 108
Characterization of novel genes in AZF regions 96
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 92
SHOX mutations detected by FISH and direct sequencing in patients with short stature 91
Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation 83
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 78
Aneuploidy screening using circulating fetal cells in maternal blood by dual-probe FISH protocol: A prospective feasibility study on a series of 172 pregnant women 78
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 75
Fluorescence in situ hybridization analysis of minimal residual disease and the relevance of the der(9) deletion in imatinib-treated patients with chronic myeloid leukemia. 74
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 67
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 66
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 65
Totale 1.082
Categoria #
all - tutte 4.269
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 4.269


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202020 0 0 0 0 0 0 0 0 0 0 19 1
2020/202181 13 0 15 0 4 17 0 0 9 12 4 7
2021/202266 0 1 1 10 2 17 0 6 2 0 7 20
2022/2023266 16 43 23 29 26 48 11 21 34 2 5 8
2023/202483 7 3 3 4 6 27 14 0 0 4 0 15
2024/2025121 17 32 22 12 6 2 7 4 17 1 1 0
Totale 1.082