IRIS
FRACCARO, MARCO
 Distribuzione geografica
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Continente #
NA - Nord America 976
EU - Europa 769
AS - Asia 565
OC - Oceania 5
AF - Africa 4
SA - Sud America 2
Totale 2.321
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Nazione #
US - Stati Uniti d'America 969
CN - Cina 561
IE - Irlanda 274
UA - Ucraina 147
FI - Finlandia 113
DE - Germania 91
SE - Svezia 56
GB - Regno Unito 31
IT - Italia 27
FR - Francia 19
CA - Canada 6
MU - Mauritius 4
AU - Australia 3
BE - Belgio 3
IN - India 2
NL - Olanda 2
NZ - Nuova Zelanda 2
RU - Federazione Russa 2
BG - Bulgaria 1
BR - Brasile 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
ES - Italia 1
HR - Croazia 1
ID - Indonesia 1
PE - Perù 1
TR - Turchia 1
Totale 2.321
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Città #
Dublin 274
Chandler 244
Jacksonville 199
Nanjing 153
Ashburn 70
Beijing 65
Nanchang 57
Shenyang 55
Hebei 52
Lawrence 44
Medford 44
Princeton 44
Changsha 42
New York 38
Jiaxing 36
Wilmington 34
Hangzhou 32
Tianjin 31
Helsinki 25
Boardman 22
Ann Arbor 16
Shanghai 15
Milan 11
Norwalk 8
Woodbridge 8
Verona 6
Des Moines 4
Los Angeles 4
Seattle 4
Toronto 4
Brussels 3
Houston 3
Jinan 3
San Francisco 3
Augusta 2
Fairfield 2
Fuzhou 2
Gunzenhausen 2
Lanzhou 2
Melbourne 2
Ningbo 2
Orange 2
Taizhou 2
Washington 2
Amsterdam 1
Auckland 1
Berlin 1
Borås 1
Brackley 1
Casier 1
Changchun 1
Codigoro 1
Grenaa 1
Kunming 1
Leawood 1
Lima 1
Monmouth Junction 1
Moscow 1
Newark 1
Nuremberg 1
Pinehaven 1
Pune 1
Redmond 1
Sacramento 1
Sarnia 1
Sofia 1
Surabaya 1
Sydney 1
São Paulo 1
Windsor 1
Zagreb 1
Totale 1.700
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Nome #
A clonal t(9;12)(q32;q21) in cultured fibroblasts from a case of Bowen's disease 100
15/15 translocation in Prader-Willi syndrome. 72
Chromosome abnormalities in Dyskeratosis congenita. 66
Cytogenetic studies in venous tissues from patients with vericose venis. 64
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1. 63
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal 63
A novel mechnaism for the origin of supernumerary marker chromosomes 62
Chromosome abnormalities in Tuberous Sclerosis. 61
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223. 61
Chromosome abnormalities and male infertility. Oligozoospermia: recent progress in andrology 61
A deletion of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis 60
Clonal chromosome abnormalities with preferential ilvolvement of chromosome 3 in patient with Porokeratosi of Mibelli. 59
"Cri du chat" syndrome due to a complex rearrangement of chromosome 5 58
Correlation between testicular tissue and H-Y phenotype in intersex patients 57
The "cat eye syndrome": dicentric small marker chromosome probably derived from a n. 22 (tetrasomy 22pter-->q11) associated with a characteristic phenotype. 57
Evidence for an ancestral alphoid domain on the long arm of human chromosome 2 57
A clonal t(),12)(q32q21) in cultured fibroblasts from a case of Bowen's disease. 57
Non fluorescent Y chromosome in a 45,X/46,XY mosaic. 56
BSu restriction of DNA from cases exhibiting sex chromosom abnormalities. 55
Xp deficiencies and female fertility 55
First trimester fetal diagnosis of gentic disorders: clinical evaluation of 250 cases 55
Premature centromere disjunction and other chromosome anomalies in Tuberous Sclerosis. 54
Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq 54
The gene for human peptidase A is on band 18q23 and shows triplex and uniplex dosage effect 54
Antenatal sex detrmination 53
XO and male phenotype 52
Shwachman syndrome and chromosome breakage. Letter to the Editor. 48
Deficiency, transposition and duplication of one 15q rwegion may be alternatively associated with Prader-Willi (or similar) syndrome. Analysis of seven cases after varying ascertainment. 47
Familial XX true hermaphroditism and the H-Y antigen. 47
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosomes 18p11.1-21.1 markers. 46
Chromosome identification and karyotypic evolution in a human melanoma cell line (MEL-41). 46
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection. 46
homozygosity mapping of the Werner syndrome locus (WRN). 45
Chromosome 15 and Prader-Willi syndrome 44
Clonal structural chromosomal rearrangements in primary fibroblastic cultures and in lymphocytes of patients with Werner's syndroe. 44
Five unusual karyotypes in Down's syndrome 44
Chromosome identification in Chinese hamster pseudodiploid cell line (CHEF-125). 43
Identification of a structurally abnormal Y chromosome. 40
X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromere. 40
Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a Glaucoma from two subjects with MEN1. 39
Turner syndrome patients are H-Y positive. 38
Cytogenetic of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasia. 38
Diagnostic application of first trimester trophobalst sampling in 100 pregnancies 37
Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430 McKusick) is at Xq28, distal to the G6PD locus 33
Totale 2.331
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Categoria #
all - tutte 6.935
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 6.935
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020659 181 284 0 26 0 33 4 30 0 67 34 0
2020/2021261 35 24 7 27 0 36 0 37 8 41 39 7
2021/2022201 2 1 3 1 2 8 1 15 10 2 33 123
2022/2023697 77 64 11 48 64 68 0 36 306 1 19 3
2023/2024219 24 35 6 13 28 78 0 26 1 8 0 0
Totale 2.331