FORABOSCO, Antonino
 Distribuzione geografica
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Continente #
NA - Nord America 4.765
AS - Asia 2.164
EU - Europa 1.718
SA - Sud America 304
AF - Africa 42
Continente sconosciuto - Info sul continente non disponibili 22
OC - Oceania 16
Totale 9.031
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Nazione #
US - Stati Uniti d'America 4.658
CN - Cina 680
SG - Singapore 607
GB - Regno Unito 537
IT - Italia 248
SE - Svezia 243
HK - Hong Kong 231
BR - Brasile 215
VN - Vietnam 195
DE - Germania 130
BD - Bangladesh 118
FI - Finlandia 103
RU - Federazione Russa 103
UA - Ucraina 94
KR - Corea 84
FR - Francia 82
TR - Turchia 74
CA - Canada 63
IN - India 38
NL - Olanda 35
BG - Bulgaria 34
AR - Argentina 24
ID - Indonesia 23
MX - Messico 18
PK - Pakistan 18
JP - Giappone 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
CR - Costa Rica 5
DK - Danimarca 5
MA - Marocco 5
MD - Moldavia 4
MY - Malesia 4
RO - Romania 4
SV - El Salvador 4
TT - Trinidad e Tobago 4
AT - Austria 3
CH - Svizzera 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
PR - Porto Rico 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
PS - Palestinian Territory 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 9.005
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Città #
Santa Clara 477
Ashburn 466
Singapore 402
Fairfield 369
Southend 336
Hefei 260
Chandler 248
Hong Kong 227
Houston 201
Woodbridge 196
Jacksonville 190
Ann Arbor 177
San Jose 165
Nyköping 134
Wilmington 130
Los Angeles 125
Dearborn 123
Chicago 121
Seattle 117
Cambridge 109
London 101
Beijing 96
Helsinki 70
Seoul 68
Ho Chi Minh City 65
New York 58
Modena 56
The Dalles 53
Hanoi 50
Council Bluffs 48
Des Moines 44
Salt Lake City 43
Izmir 38
San Diego 38
Lauterbourg 36
Princeton 35
Moscow 34
Buffalo 33
Shanghai 33
Sofia 32
Eugene 30
Dallas 26
Milan 26
Elk Grove Village 24
Tampa 23
Vancouver 21
Amsterdam 20
Rome 18
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
Calgary 7
Kunming 7
Miami 7
Newark 7
Nuremberg 7
Santiago 7
Ankara 6
Atlanta 6
Baltimore 6
Bologna 6
Changsha 6
Chennai 6
Hounslow 6
Jinan 6
Norwalk 6
Sydney 6
Towson 6
Zhengzhou 6
Amman 5
Brooklyn 5
Charlotte 5
Totale 6.231
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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 362
Emx2 developmental expression in the primordia of the reproductive and excretory systems 347
Agenesis of the scapula in Emx2 homozygous mutants 331
Pure segmental trisomy 1q42-qter in a boy with a severe phenotype 331
The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia. 325
Genes and translocations involved in POF 317
SHOX gene in Leri-Weill syndrome and in idiopathic short stature 315
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material 311
Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmel syndrome 297
SHORT STATURE HOMEOBOX-CONTAINING GENE AND IDIOPATHIC SHORT STATURE 297
Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: Patient report and review of the literature 296
Age-specific risk of fetal loss post second trimester amniocentesis: analysis of 5043 cases 290
Morphometric study of human neonatal ovary. 281
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination 273
Morphometric Study Of The Human Ovary During Compartmentalization 265
Unexpected phenotype in a boy with trisomy of the SHOX gene. 241
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses 231
Apoptosis in different stages of human oogenesis. 231
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele 229
Developmental Pathways Of Vertebral Centra And Neural Arches In Human Embryos And Fetuses 228
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness 227
Foxl2 is required for commitment to ovary differentiation 212
FETAL THYMIC DIFFERENTIATION IN DOWNS-SYNDROME 208
Human neonatal ovary: proposal of a tree- dimensional model. 203
Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe 203
Determination and stability of sex 199
Il gene SHOX e il suo ruolo nei disturbi dell’accrescimento 199
Quantitative study of definitive histogenesis in normal and trisomy 21 ovaries. 189
Aging of oocyte, ovary, and human reproduction 183
Growth patterns of human ovarian volume during intrauterine and postnatal organogenesis 167
Atrofia ottica dominante: studio genetico clinico 161
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
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development 150
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.] 149
The use of non-physiological conditions to isolate fetal cells from maternal blood 130
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 96
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 9.031
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Categoria #
all - tutte 37.042
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 37.042
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022558 0 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
2025/20263.292 260 146 284 396 576 269 258 157 254 286 197 209
2026/2027128 128 0 0 0 0 0 0 0 0 0 0 0
Totale 9.031