TIEPOLO, LUCIANO
 Distribuzione geografica
Continente #
NA - Nord America 518
EU - Europa 433
AS - Asia 283
AF - Africa 2
OC - Oceania 1
Totale 1.237
Nazione #
US - Stati Uniti d'America 514
CN - Cina 272
IE - Irlanda 152
UA - Ucraina 97
DE - Germania 59
FI - Finlandia 58
GB - Regno Unito 21
IT - Italia 20
SE - Svezia 11
FR - Francia 9
JP - Giappone 5
CA - Canada 4
BE - Belgio 2
LA - Repubblica Popolare Democratica del Laos 2
MU - Mauritius 2
TR - Turchia 2
CZ - Repubblica Ceca 1
IR - Iran 1
MK - Macedonia 1
NZ - Nuova Zelanda 1
PL - Polonia 1
RU - Federazione Russa 1
SG - Singapore 1
Totale 1.237
Città #
Dublin 152
Chandler 151
Jacksonville 113
Nanjing 84
Beijing 31
Nanchang 26
Wilmington 25
Ashburn 24
Hebei 24
Lawrence 21
Medford 21
Princeton 21
Changsha 19
Shanghai 18
Helsinki 16
Jiaxing 16
Shenyang 15
Ann Arbor 14
Tianjin 13
Hangzhou 12
Boardman 11
New York 6
Verona 6
Milan 5
Tokyo 5
Woodbridge 5
San Francisco 4
Lanzhou 3
Norwalk 3
Toronto 3
Auburn Hills 2
Berlin 2
Brussels 2
Jinan 2
Los Angeles 2
St Louis 2
Ancona 1
Andover 1
Auckland 1
Baltimore 1
Brno 1
Düsseldorf 1
Fuzhou 1
Haikou 1
Houston 1
Kunming 1
Moscow 1
Ningbo 1
Pavia 1
Seattle 1
Singapore 1
Skopje 1
Stanton 1
Vientiane 1
Warsaw 1
Windsor 1
Zhengzhou 1
Totale 900
Nome #
XX sex reversal, palmoplantar keratoderma, and predisposition to squamous cell carcinoma: genetic analysis in one family. 86
A novel mutation and novel features in Nijmegen breakage syndrome. 75
Citochimica, autoradiografia e ultrastruttura di cellule della granulosa ovarica umana "in vitro". 75
Comment on: Corpus callosum hypoplasia and associated brain anomalies in Nijmegen breakage syndrome. 73
XX sex reversal, palmoplantar keratoderma, and predisposition to squamous cell carcinoma: genetic analysis in one family. 64
Ribosomal RNA in infertile male carriers of Robertsonian translocations 63
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223. 62
Chromosome abnormalities and male infertility. Oligozoospermia: recent progress in andrology 61
Localization of factors controlling spermatogenesis in the nonfluoresecent portion of the human Y chromosome long arm. 58
The "cat eye syndrome": dicentric small marker chromosome probably derived from a n. 22 (tetrasomy 22pter-->q11) associated with a characteristic phenotype. 57
Reduced phenotypic effetc of partial trisomy 1q in a X/1 translocation. 57
Orign and clinical significance of inv dup(15) 57
BSu restriction of DNA from cases exhibiting sex chromosom abnormalities. 56
Nullisomy for the distal portion of Xp in a male child with a X/Y translocation. 56
Immunodeficiency, centromeric heterochromatin instability of chromosome 1, 9 and 16 and facial anomalies: the ICF syndrome. 56
Frequencies and types of chromosome abnormalities associated with human male infertility 55
Agenesis of corpus callosum, ocular and skeletal anomalies (x-linked dominant Aicardi's syndrome) 50
Genetic heterogeneity for a Nijmegen Breakage-like Syndrome 49
Familial XX true hermaphroditism and the H-Y antigen. 48
Chromosome instability and nibrin protein variants in NBS heterozygotes. 42
Identification of a structurally abnormal Y chromosome. 40
Totale 1.240
Categoria #
all - tutte 3.927
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 3.927


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020319 81 125 0 17 1 19 4 21 0 28 23 0
2020/2021145 19 18 1 17 1 19 1 25 2 20 21 1
2021/202296 0 1 0 0 1 3 0 7 5 2 15 62
2022/2023394 30 36 14 20 45 39 0 21 176 2 7 4
2023/2024116 8 37 3 5 14 17 1 9 4 3 5 10
Totale 1.240