FORABOSCO, Antonino
 Distribuzione geografica
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Continente #
NA - Nord America 4.676
AS - Asia 2.140
EU - Europa 1.701
SA - Sud America 303
AF - Africa 42
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 1
Totale 8.879
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Nazione #
US - Stati Uniti d'America 4.584
CN - Cina 676
SG - Singapore 602
GB - Regno Unito 536
SE - Svezia 243
IT - Italia 235
HK - Hong Kong 230
BR - Brasile 214
VN - Vietnam 195
DE - Germania 130
BD - Bangladesh 104
FI - Finlandia 103
RU - Federazione Russa 103
UA - Ucraina 93
KR - Corea 84
FR - Francia 82
TR - Turchia 74
CA - Canada 54
IN - India 38
NL - Olanda 35
BG - Bulgaria 34
AR - Argentina 24
ID - Indonesia 23
PK - Pakistan 18
JP - Giappone 17
MX - Messico 17
AU - Australia 16
ES - Italia 16
IE - Irlanda 16
PL - Polonia 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
VE - Venezuela 7
CZ - Repubblica Ceca 6
JO - Giordania 6
KE - Kenya 6
NP - Nepal 6
UY - Uruguay 6
MA - Marocco 5
MD - Moldavia 4
MY - Malesia 4
RO - Romania 4
TT - Trinidad e Tobago 4
AT - Austria 3
CH - Svizzera 3
CR - Costa Rica 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
EG - Egitto 3
ET - Etiopia 3
GT - Guatemala 3
IR - Iran 3
KZ - Kazakistan 3
NO - Norvegia 3
PT - Portogallo 3
TH - Thailandia 3
UZ - Uzbekistan 3
GR - Grecia 2
HN - Honduras 2
HU - Ungheria 2
KH - Cambogia 2
OM - Oman 2
SV - El Salvador 2
TN - Tunisia 2
TW - Taiwan 2
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BJ - Benin 1
BO - Bolivia 1
CV - Capo Verde 1
CY - Cipro 1
DZ - Algeria 1
EU - Europa 1
GE - Georgia 1
GH - Ghana 1
IS - Islanda 1
JM - Giamaica 1
KG - Kirghizistan 1
LB - Libano 1
LK - Sri Lanka 1
LV - Lettonia 1
MK - Macedonia 1
MT - Malta 1
MU - Mauritius 1
NI - Nicaragua 1
PA - Panama 1
PE - Perù 1
PR - Porto Rico 1
PS - Palestinian Territory 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 8.874
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Città #
Santa Clara 475
Ashburn 453
Singapore 401
Fairfield 369
Southend 336
Hefei 260
Chandler 248
Hong Kong 226
Houston 201
Woodbridge 196
Jacksonville 190
Ann Arbor 177
San Jose 164
Nyköping 134
Wilmington 130
Dearborn 123
Los Angeles 123
Chicago 120
Seattle 116
Cambridge 109
London 101
Beijing 96
Helsinki 70
Seoul 68
Ho Chi Minh City 65
Modena 56
New York 56
The Dalles 52
Hanoi 50
Council Bluffs 48
Des Moines 44
Salt Lake City 43
Izmir 38
San Diego 38
Lauterbourg 36
Princeton 35
Moscow 34
Shanghai 33
Buffalo 32
Sofia 32
Eugene 30
Dallas 25
Elk Grove Village 24
Tampa 23
Milan 22
Vancouver 21
Amsterdam 20
Rome 17
Dublin 16
Orem 16
Seongnam 13
São Paulo 13
Columbus 12
Haiphong 12
Lancaster 12
Nanjing 12
Phoenix 12
Falls Church 11
Rio de Janeiro 11
Boardman 10
Manchester 10
Toronto 10
Warsaw 10
Augusta 9
Munich 9
Sterling 9
Stockholm 9
Bremen 8
Brussels 8
Da Nang 8
Frankfurt am Main 8
Kent 8
Kilburn 8
Miano 8
Philadelphia 8
San Mateo 8
Tokyo 8
Altamura 7
Boston 7
Kunming 7
Miami 7
Nuremberg 7
Santiago 7
Ankara 6
Baltimore 6
Bologna 6
Changsha 6
Chennai 6
Hounslow 6
Jinan 6
Newark 6
Norwalk 6
Sydney 6
Towson 6
Zhengzhou 6
Amman 5
Atlanta 5
Calgary 5
Detroit 5
Dhaka 5
Totale 6.195
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Nome #
Mouse ovary developmental RNA and protein markers from gene expression profiling 374
Barber-Say syndrome: Report of a new case 361
Emx2 developmental expression in the primordia of the reproductive and excretory systems 346
Agenesis of the scapula in Emx2 homozygous mutants 330
Pure segmental trisomy 1q42-qter in a boy with a severe phenotype 329
The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia. 324
Genes and translocations involved in POF 317
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material 308
SHOX gene in Leri-Weill syndrome and in idiopathic short stature 305
Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: Patient report and review of the literature 295
SHORT STATURE HOMEOBOX-CONTAINING GENE AND IDIOPATHIC SHORT STATURE 294
Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmel syndrome 293
Age-specific risk of fetal loss post second trimester amniocentesis: analysis of 5043 cases 287
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination 271
Morphometric study of human neonatal ovary. 262
Morphometric Study Of The Human Ovary During Compartmentalization 261
Unexpected phenotype in a boy with trisomy of the SHOX gene. 240
Apoptosis in different stages of human oogenesis. 228
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele 227
Developmental Pathways Of Vertebral Centra And Neural Arches In Human Embryos And Fetuses 226
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness 222
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses 210
Foxl2 is required for commitment to ovary differentiation 208
FETAL THYMIC DIFFERENTIATION IN DOWNS-SYNDROME 204
Human neonatal ovary: proposal of a tree- dimensional model. 201
Il gene SHOX e il suo ruolo nei disturbi dell’accrescimento 199
Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe 199
Determination and stability of sex 191
Quantitative study of definitive histogenesis in normal and trisomy 21 ovaries. 189
Aging of oocyte, ovary, and human reproduction 181
Growth patterns of human ovarian volume during intrauterine and postnatal organogenesis 161
Atrofia ottica dominante: studio genetico clinico 160
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] 157
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.] 148
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development 145
The use of non-physiological conditions to isolate fetal cells from maternal blood 126
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 95
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 8.900
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Categoria #
all - tutte 36.112
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 36.112
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202142 0 0 0 0 0 0 0 0 0 0 0 42
2021/2022566 8 79 59 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
2025/20263.289 260 146 284 396 576 269 258 157 254 286 197 206
Totale 8.900