FORABOSCO, Antonino
 Distribuzione geografica
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Continente #
NA - Nord America 2.628
EU - Europa 1.128
AS - Asia 371
OC - Oceania 7
SA - Sud America 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 4.138
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Nazione #
US - Stati Uniti d'America 2.615
GB - Regno Unito 435
SE - Svezia 210
CN - Cina 137
IT - Italia 121
DE - Germania 98
UA - Ucraina 85
HK - Hong Kong 76
TR - Turchia 61
SG - Singapore 58
FI - Finlandia 50
BG - Bulgaria 31
FR - Francia 31
KR - Corea 17
IE - Irlanda 13
IN - India 13
CA - Canada 11
ES - Italia 8
RU - Federazione Russa 8
AU - Australia 7
BE - Belgio 7
LT - Lituania 6
NL - Olanda 6
CZ - Repubblica Ceca 5
PL - Polonia 4
AR - Argentina 2
CH - Svizzera 2
ID - Indonesia 2
IR - Iran 2
JP - Giappone 2
MX - Messico 2
MY - Malesia 2
NO - Norvegia 2
BR - Brasile 1
DK - Danimarca 1
EU - Europa 1
GR - Grecia 1
HU - Ungheria 1
IS - Islanda 1
MD - Moldavia 1
PH - Filippine 1
RO - Romania 1
Totale 4.138
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Città #
Fairfield 367
Southend 336
Chandler 248
Houston 196
Woodbridge 196
Jacksonville 189
Ann Arbor 177
Ashburn 172
Nyköping 134
Wilmington 126
Dearborn 123
Cambridge 109
Seattle 107
Hong Kong 76
Modena 56
Des Moines 44
Beijing 40
Izmir 38
Princeton 35
Singapore 35
San Diego 34
Sofia 31
Eugene 30
London 21
Shanghai 21
Helsinki 20
New York 20
Dublin 13
Seongnam 13
Falls Church 11
Nanjing 11
Milan 9
Augusta 8
Bremen 8
Kilburn 8
San Mateo 8
Boardman 7
San Jose 7
Brussels 6
Hounslow 6
Kunming 6
Norwalk 6
Toronto 6
Rome 5
Saint Petersburg 5
Bologna 4
Brno 4
Jinan 4
Leawood 4
Los Angeles 4
Monmouth Junction 4
Philadelphia 4
Prescot 4
Saint Catharines 4
Auburn Hills 3
Brescia 3
Chiswick 3
Frankfurt am Main 3
Guangzhou 3
Munich 3
Parma 3
Redwood City 3
Ardabil 2
Chicago 2
Fermignano 2
Ferrara di Monte Baldo 2
Fremont 2
Gjøvik 2
Groningen 2
Hangzhou 2
Hefei 2
Jakarta 2
Jiaxing 2
Las Vegas 2
Lusciano 2
Mcallen 2
Mumbai 2
Munro 2
Nanchang 2
Quartu Sant'Elena 2
Rimini 2
Scottsdale 2
Seoul 2
Southwark 2
Tulare 2
Verona 2
Vigo 2
Zhengzhou 2
Zurich 2
Adelaide 1
Albano 1
Albuquerque 1
Alicante 1
Arvada 1
Bangalore 1
Bloomington 1
Bogen 1
Bondeno 1
Borås 1
Boston 1
Totale 3.249
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Nome #
Barber-Say syndrome: Report of a new case 184
SHOX gene in Leri-Weill syndrome and in idiopathic short stature 180
Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: Patient report and review of the literature 175
Emx2 developmental expression in the primordia of the reproductive and excretory systems 172
Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmel syndrome 167
Genes and translocations involved in POF 166
Age-specific risk of fetal loss post second trimester amniocentesis: analysis of 5043 cases 161
Agenesis of the scapula in Emx2 homozygous mutants 159
Mouse ovary developmental RNA and protein markers from gene expression profiling 151
SHORT STATURE HOMEOBOX-CONTAINING GENE AND IDIOPATHIC SHORT STATURE 149
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material 145
Morphometric Study Of The Human Ovary During Compartmentalization 144
Pure segmental trisomy 1q42-qter in a boy with a severe phenotype 144
Morphometric study of human neonatal ovary. 143
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination 142
Unexpected phenotype in a boy with trisomy of the SHOX gene. 137
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness 131
Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe 130
The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia. 130
Developmental Pathways Of Vertebral Centra And Neural Arches In Human Embryos And Fetuses 127
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses 121
FETAL THYMIC DIFFERENTIATION IN DOWNS-SYNDROME 115
Apoptosis in different stages of human oogenesis. 111
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele 102
Quantitative study of definitive histogenesis in normal and trisomy 21 ovaries. 98
Human neonatal ovary: proposal of a tree- dimensional model. 89
Il gene SHOX e il suo ruolo nei disturbi dell’accrescimento 88
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.] 85
Atrofia ottica dominante: studio genetico clinico 81
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] 77
Foxl2 is required for commitment to ovary differentiation 28
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development 24
Growth patterns of human ovarian volume during intrauterine and postnatal organogenesis 23
Determination and stability of sex 23
Aging of oocyte, ovary, and human reproduction 17
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 7
The use of non-physiological conditions to isolate fetal cells from maternal blood 7
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 4.159
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Categoria #
all - tutte 19.934
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 19.934
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020863 78 59 33 60 100 122 134 86 81 19 41 50
2020/2021586 44 18 47 49 74 27 61 81 22 74 47 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
2024/202555 55 0 0 0 0 0 0 0 0 0 0 0
Totale 4.159