MATTINA, Teresa
 Distribuzione geografica
Continente #
EU - Europa 84
NA - Nord America 46
AS - Asia 10
OC - Oceania 1
SA - Sud America 1
Totale 142
Nazione #
IT - Italia 43
US - Stati Uniti d'America 42
IE - Irlanda 22
VN - Vietnam 6
CZ - Repubblica Ceca 5
DE - Germania 5
FR - Francia 5
CA - Canada 2
IN - India 2
PA - Panama 2
AU - Australia 1
CO - Colombia 1
FI - Finlandia 1
GB - Regno Unito 1
GR - Grecia 1
IL - Israele 1
MY - Malesia 1
RU - Federazione Russa 1
Totale 142
Città #
Dublin 22
Catania 19
Bremen 5
Dong Ket 5
Fleming Island 5
Aci Catena 3
Duluth 3
Florence 3
Palermo 3
Vittoria 3
Biloxi 2
Houston 2
Juan Díaz 2
Miami 2
Milpitas 2
Oklahoma City 2
Rome 2
Ashburn 1
Benton 1
Boardman 1
Calgary 1
Cascina 1
Cheras 1
Châtellerault 1
Coimbatore 1
Corciano 1
Council Bluffs 1
Hamilton 1
Hanoi 1
Helsinki 1
Iowa Falls 1
Lake Forest 1
Los Angeles 1
Lyon 1
Manerbio 1
Milan 1
Monterey Park 1
New Hyde Park 1
Orlando 1
Paris 1
Pittsburgh 1
Reggio Nell'emilia 1
Rehovot 1
Santa Clara 1
Seattle 1
St Louis 1
Tampa 1
Vista 1
Williamsburg 1
Totale 117
Nome #
Partial trisomy 21 map: Ten cases further supporting the highly restricted Down syndrome critical region (HR-DSCR) on human chromosome 21, file dfe4d22b-a676-bb0a-e053-d805fe0a78d9 54
Biallelic intragenic duplication in ADGRB3 (BAI3) gene associated with intellectual disability, cerebellar atrophy, and behavioral disorder, file dfe4d22b-669c-bb0a-e053-d805fe0a78d9 26
Phenotypic Expansion in Nasu-Hakola Disease: Immunological Findings in Three Patients and Proposal of a Unifying Pathogenic Hypothesis, file dfe4d22b-a677-bb0a-e053-d805fe0a78d9 13
Chromosome 15 structural abnormalities: effect on the IGF1R gene expression and function, file dfe4d228-b7c6-bb0a-e053-d805fe0a78d9 7
Early Motor Delay: An Outstanding, Initial Sign of Osteogenesis Imperfecta Type 1, file dfe4d228-9317-bb0a-e053-d805fe0a78d9 6
A Customized Next-Generation Sequencing-Based Panel to Identify Novel Genetic Variants in Dementing Disorders: A Pilot Study, file dfe4d22d-cea6-bb0a-e053-d805fe0a78d9 6
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants, file dfe4d229-93e6-bb0a-e053-d805fe0a78d9 5
The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant, file dfe4d22b-b2dc-bb0a-e053-d805fe0a78d9 5
Familial 18q12.2 deletion supports the role of RNA-bindingprotein CELF4 in autism spectrum disorders, file 7d3b35d9-6402-44e4-a455-12d9fe9fa611 4
Melorheostosis and Osteopoikilosis Clinical and Molecular Description of an Italian Case Series, file dfe4d229-e320-bb0a-e053-d805fe0a78d9 4
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani, file dfe4d229-dd62-bb0a-e053-d805fe0a78d9 3
Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform, file dfe4d227-2f96-bb0a-e053-d805fe0a78d9 2
Principi di genetica generale ed ereditarietà, file dfe4d227-4d20-bb0a-e053-d805fe0a78d9 2
IGF-1R: it is involved in etiopathogenesis of human gonadal abnormalities?, file dfe4d227-605f-bb0a-e053-d805fe0a78d9 2
Mild cystic fibrosis in patients with the rare P5L CFTR mutation, file dfe4d227-2cb6-bb0a-e053-d805fe0a78d9 1
"Balanced" complex rearrangements: how many are really balanced?, file dfe4d227-39ba-bb0a-e053-d805fe0a78d9 1
Decreased expression of GRAF1/OPHN-1-L in the X-linked alpha thalassemia mental retardation syndrome, file dfe4d227-a3d9-bb0a-e053-d805fe0a78d9 1
Familial 18q12.2 deletion supports the role of RNA-binding protein CELF4 in autism spectrum disorders., file dfe4d22a-dff3-bb0a-e053-d805fe0a78d9 1
Small supernumerary marker chromosomes: A legacy of trisomy rescue?, file dfe4d22b-a675-bb0a-e053-d805fe0a78d9 1
Clinical correlates in children with autism spectrum disorder and CNVs: Systematic investigation in a clinical setting, file dfe4d22b-de19-bb0a-e053-d805fe0a78d9 1
Familiar osteopoikilosis: Case report with differential diagnosis and review of the literature, file dfe4d22e-3200-bb0a-e053-d805fe0a78d9 1
Totale 146
Categoria #
all - tutte 261
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 261


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203 0000 00 00 0021
2020/202118 1100 20 22 3016
2021/202228 2112 36 04 3222
2022/202396 4038 2020 1812 11000
Totale 146