FORABOSCO, Antonino
 Distribuzione geografica
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Continente #
NA - Nord America 5.626
AS - Asia 2.175
EU - Europa 1.751
SA - Sud America 311
AF - Africa 44
Continente sconosciuto - Info sul continente non disponibili 23
OC - Oceania 17
Totale 9.947
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Nazione #
US - Stati Uniti d'America 5.476
CN - Cina 681
SG - Singapore 611
GB - Regno Unito 543
IT - Italia 264
SE - Svezia 243
HK - Hong Kong 231
BR - Brasile 222
VN - Vietnam 195
DE - Germania 131
BD - Bangladesh 120
RU - Federazione Russa 105
FI - Finlandia 103
UA - Ucraina 95
CA - Canada 87
KR - Corea 85
FR - Francia 84
TR - Turchia 74
IN - India 38
NL - Olanda 37
BG - Bulgaria 34
AR - Argentina 24
ID - Indonesia 24
MX - Messico 19
PK - Pakistan 18
AU - Australia 17
JP - Giappone 17
PL - Polonia 17
ES - Italia 16
IE - Irlanda 16
ZA - Sudafrica 15
CL - Cile 14
CO - Colombia 14
EC - Ecuador 12
LT - Lituania 10
SA - Arabia Saudita 10
AE - Emirati Arabi Uniti 9
BE - Belgio 9
IQ - Iraq 9
PH - Filippine 9
PY - Paraguay 9
CR - Costa Rica 7
GT - Guatemala 7
VE - Venezuela 7
CZ - Repubblica Ceca 6
DK - Danimarca 6
JM - Giamaica 6
JO - Giordania 6
KE - Kenya 6
NP - Nepal 6
UY - Uruguay 6
MA - Marocco 5
SV - El Salvador 5
HN - Honduras 4
MD - Moldavia 4
MY - Malesia 4
RO - Romania 4
TH - Thailandia 4
TT - Trinidad e Tobago 4
AT - Austria 3
CH - Svizzera 3
DO - Repubblica Dominicana 3
EG - Egitto 3
ET - Etiopia 3
IR - Iran 3
KZ - Kazakistan 3
NO - Norvegia 3
PR - Porto Rico 3
PT - Portogallo 3
UZ - Uzbekistan 3
GR - Grecia 2
HU - Ungheria 2
KH - Cambogia 2
NI - Nicaragua 2
OM - Oman 2
SC - Seychelles 2
TN - Tunisia 2
TW - Taiwan 2
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BJ - Benin 1
BO - Bolivia 1
BS - Bahamas 1
CU - Cuba 1
CV - Capo Verde 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
DZ - Algeria 1
EE - Estonia 1
EU - Europa 1
GE - Georgia 1
GH - Ghana 1
IL - Israele 1
IS - Islanda 1
KG - Kirghizistan 1
LB - Libano 1
LK - Sri Lanka 1
LV - Lettonia 1
MK - Macedonia 1
MT - Malta 1
Totale 9.915
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Città #
Ashburn 671
Santa Clara 486
Singapore 404
Fairfield 369
Southend 336
Hefei 260
Chandler 248
Hong Kong 227
San Jose 222
Houston 202
Woodbridge 197
Jacksonville 190
Ann Arbor 178
Nyköping 134
Los Angeles 133
Council Bluffs 130
Wilmington 130
Chicago 124
Dearborn 123
Seattle 119
Cambridge 109
London 103
Beijing 97
Helsinki 70
Seoul 69
Ho Chi Minh City 65
New York 65
Modena 56
The Dalles 55
Hanoi 50
Salt Lake City 46
Des Moines 45
San Diego 39
Izmir 38
Buffalo 36
Lauterbourg 36
Princeton 35
Moscow 34
Shanghai 33
Sofia 32
Dallas 31
Milan 31
Eugene 30
Elk Grove Village 24
Tampa 23
Vancouver 22
Amsterdam 21
Phoenix 20
Rome 19
São Paulo 19
Toronto 18
Columbus 17
Orem 17
Dublin 16
Atlanta 14
Seongnam 13
Haiphong 12
Lancaster 12
Nanjing 12
Falls Church 11
Rio de Janeiro 11
Boardman 10
Manchester 10
Newark 10
Warsaw 10
Augusta 9
Boston 9
Munich 9
San Francisco 9
San Mateo 9
Sterling 9
Stockholm 9
Bremen 8
Brussels 8
Da Nang 8
Denver 8
Frankfurt am Main 8
Kent 8
Kilburn 8
Las Vegas 8
Miano 8
Norfolk 8
Philadelphia 8
Tokyo 8
Altamura 7
Calgary 7
Kunming 7
Miami 7
Nuremberg 7
Santiago 7
Ankara 6
Baltimore 6
Bologna 6
Brooklyn 6
Changsha 6
Charlotte 6
Chennai 6
Guatemala City 6
Honolulu 6
Hounslow 6
Totale 6.690
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Nome #
SHOX gene in Leri-Weill syndrome and in idiopathic short stature 497
Mouse ovary developmental RNA and protein markers from gene expression profiling 403
Barber-Say syndrome: Report of a new case 386
Emx2 developmental expression in the primordia of the reproductive and excretory systems 375
Genes and translocations involved in POF 342
Agenesis of the scapula in Emx2 homozygous mutants 341
Pure segmental trisomy 1q42-qter in a boy with a severe phenotype 341
The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia. 334
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material 332
Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmel syndrome 318
Age-specific risk of fetal loss post second trimester amniocentesis: analysis of 5043 cases 316
SHORT STATURE HOMEOBOX-CONTAINING GENE AND IDIOPATHIC SHORT STATURE 311
Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: Patient report and review of the literature 305
Morphometric study of human neonatal ovary. 298
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination 292
Morphometric Study Of The Human Ovary During Compartmentalization 283
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses 255
Apoptosis in different stages of human oogenesis. 255
Foxl2 is required for commitment to ovary differentiation 249
Unexpected phenotype in a boy with trisomy of the SHOX gene. 248
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness 248
Determination and stability of sex 247
Developmental Pathways Of Vertebral Centra And Neural Arches In Human Embryos And Fetuses 242
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele 239
Human neonatal ovary: proposal of a tree- dimensional model. 233
FETAL THYMIC DIFFERENTIATION IN DOWNS-SYNDROME 232
Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe 213
Il gene SHOX e il suo ruolo nei disturbi dell’accrescimento 210
Quantitative study of definitive histogenesis in normal and trisomy 21 ovaries. 208
Aging of oocyte, ovary, and human reproduction 206
Sul test di esclusione del colore. - I Valutazione della concentrazione ottimale [On the dye exclusion of test cell vitality. I. Evaluation of the optimal concentration] 196
Sul test di esclusione del colore. - II Influenza di sostanze macromolecolari neutre. [On the dye exclusion test of cell vitality. II. Influence of neutral macromolecular substances.] 190
Growth patterns of human ovarian volume during intrauterine and postnatal organogenesis 182
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development 175
Atrofia ottica dominante: studio genetico clinico 171
The use of non-physiological conditions to isolate fetal cells from maternal blood 137
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 111
A NEW FAMILY WITH CHORIORETINAL DYSTROPHY, SPINOCEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM (BOUCHER-NEUHAUSER SYNDROME) 2
Micromanipulation of cryopreserved embryos and cryopreservation of micromanipulated embryos in PGD 1
PLAC1, an Xq26 gene with placenta-specific expression 1
Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements 1
Analysis of fetal sex in TCC sample DNA: A contribution to the validation of this approach 1
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 1
RING CHROMOSOME 7 - REPORT OF THE 5TH CASE 1
MOLECULAR STRATEGIES IN GENETIC DIAGNOSIS OF TRANSTHYRETIN-RELATED HEREDITARY AMYLOIDOSIS 1
THE PREDICTIVE VALUE OF CYTOGENETIC DIAGNOSIS AFTER CVS BASED ON 4860 CASES WITH BOTH DIRECT AND CULTURE METHODS 1
DISTAL 12P DELETION IN A STILLBORN INFANT 1
CLONAL STRUCTURAL CHROMOSOMAL REARRANGEMENTS IN LYMPHOCYTES OF 4 PATIENTS WITH WERNERS SYNDROME 1
A NEW MUTATION (TTR ALA-47) IN THE TRANSTHYRETIN GENE ASSOCIATED WITH HEREDITARY AMYLOIDOSIS 1
Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution. 1
Noonan-like syndrome with loose anagen hair: a new syndrome? 1
Molecular analysis of the Rett syndrome using cDNA synapsin I as a probe. 1
THE GROWTH OF LONG BONES IN HUMAN EMBRYOLOGICAL AND FETAL UPPER LIMBS AND ITS RELATIONSHIP TO OTHER DEVELOPMENTAL PATTERNS 1
ANDROGEN RECEPTOR GENE (CAG)N REPEAT ANALYSIS IN THE DIFFERENTIAL-DIAGNOSIS BETWEEN KENNEDY DISEASE AND OTHER MOTONEURON DISORDERS 1
A QUANTITATIVE STUDY ON THE SPATIAL AND TEMPORAL OSSIFICATION PATTERNS OF VERTEBRAL CENTRA AND NEURAL ARCHES AND THEIR RELATIONSHIP TO THE FETAL AGE 1
Meiotic and developmental competence of mouse antral oocytes 1
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 1
On the assessment of the growth patterns in human fetal limbs: Longitudinal measurements and allometric analysis 1
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 1
NORMAL SIZE OF HANDS AND FEET IN PRADER-WILLI SYNDROME 1
Characterization of the biophysical properties of human erythroblasts as a preliminary step to the isolation of fetal erythroblasts from maternal peripheral blood for non invasive prenatal genetic investigation 1
Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome 1
Totale 9.947
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Categoria #
all - tutte 39.744
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 39.744
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022420 0 0 0 46 24 26 38 17 63 27 114 65
2022/2023715 85 82 47 71 66 137 12 71 80 6 35 23
2023/2024388 8 36 25 31 90 18 57 44 15 9 25 30
2024/20251.507 67 13 32 90 334 228 95 87 146 70 175 170
2025/20263.292 260 146 284 396 576 269 258 157 254 286 197 209
2026/20271.044 128 289 239 388 0 0 0 0 0 0 0 0
Totale 9.947