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Patruno, Margherita
38
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Online (38)
Mediatypes
Articles (Online) (16)
OpenAccess-fulltext (22)
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1
SIUrO best practice recommendations to optimize BRCA 1/2 ge..:
Cimadamore, Alessia
;
Rescigno, Pasquale
;
Conteduca, Vincenza
...
Virchows Archiv. 483 (2023) 5 - p. 579-589 , 2023
Link:
https://doi.org/10.1007/..
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2
Remote vs in-person BRCA1/2 non-carriers test disclosure: p..:
Costanzo, Silvia
;
De Summa, Simona
;
Maurmo, Leonarda
...
Familial Cancer. 22 (2022) 1 - p. 43-48 , 2022
Link:
https://doi.org/10.1007/..
?
3
Detection of Germline Variants in 450 Breast/Ovarian Cancer..:
Guglielmi, Chiara
;
Scarpitta, Rosa
;
Gambino, Gaetana
...
International Journal of Molecular Sciences. 22 (2021) 14 - p. 7693 , 2021
Link:
https://doi.org/10.3390/..
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4
Spectrum of Germline Pathogenic Variants in BRCA1/2 Genes i..:
Patruno, Margherita
;
De Summa, Simona
;
Resta, Nicoletta
...
Cancers. 13 (2021) 18 - p. 4714 , 2021
Link:
https://doi.org/10.3390/..
?
5
Blood Arsenic Levels as a Marker of Breast Cancer Risk amon..:
Marciniak, Wojciech
;
Matoušek, Tomáš
;
Domchek, Susan
...
Cancers. 13 (2021) 13 - p. 3345 , 2021
Link:
https://doi.org/10.3390/..
?
6
Somatic BRCA Mutation in a Cholangiocarcinoma Patient for H..:
Paradiso, Angelo Virgilio
;
Patruno, Margherita
;
Digennaro, Maria
...
Frontiers in Oncology. 10 (2020) - p. , 2020
Link:
https://doi.org/10.3389/..
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7
Accurate Classification of NF1 Gene Variants in 84 Italian ..:
Stella, Alessandro
;
Lastella, Patrizia
;
Loconte, Daria Carmela
...
Genes. 9 (2018) 4 - p. 216 , 2018
Link:
https://doi.org/10.3390/..
?
8
Two novel cases of compound heterozygous mutations in mitof..:
Geroldi, Alessandro
;
Lastella, Patrizia
;
Patruno, Margherita
...
Neuromuscular Disorders. 27 (2017) 4 - p. 377-381 , 2017
Link:
https://doi.org/10.1016/..
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9
Familly with two different cases of post- and pre-natal l1 ..:
Bukvic, Nenad
;
Boaretto, Francesca
;
Loverro, Giuseppe
...
Genetika; ABI Genetika. 48 (2016) 2 - p. 753-760 , 2016
Link:
https://doi.org/10.2298/..
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10
Molecular and Functional Characterization of Three Differen..:
Loconte, Daria C.
;
Grossi, Valentina
;
Bozzao, Cristina
...
PLOS ONE. 10 (2015) 4 - p. e0123092 , 2015
Link:
https://doi.org/10.1371/..
?
11
A rare MSH2 mutation causes defective binding to hMSH6, nor..:
Loconte, Daria Carmela
;
Patruno, Margherita
;
Lastella, Patrizia
...
Human Pathology. 45 (2014) 10 - p. 2162-2167 , 2014
Link:
https://doi.org/10.1016/..
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12
Characterization of the rs2802292 SNP identifies FOXO3Aas a..:
Forte, Giovanna
;
Grossi, Valentina
;
Celestini, Valentina
...
BMC Cancer. 14 (2014) 1 - p. , 2014
Link:
https://doi.org/10.1186/..
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13
Survey of KRAS, BRAF and PIK3CA mutational status in 209 co..:
Bozzao, Cristina
;
Varvara, Dora
;
Piglionica, Marilidia
...
The International Journal of Biological Markers. 27 (2012) 4 - p. 366-374 , 2012
Link:
https://doi.org/10.5301/..
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14
Identification and surveillance of 19 Lynch syndrome famili..:
Lastella, Patrizia
;
Patruno, Margherita
;
Forte, Giovanna
...
Familial Cancer. 10 (2011) 2 - p. 285-295 , 2011
Link:
https://doi.org/10.1007/..
?
15
Detection of Germline Variants in 450 Breast/Ovarian Cancer..:
Guglielmi, Chiara
;
Scarpitta, Rosa
;
Gambino, Gaetana
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305371/. , 2021
Link:
http://www.ncbi.nlm.nih...
1-15