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1 . Academic Journal
Morphological, Histochemical, Immunohistochemical, and Ultrastructural Characterization of Tumors and Dysplastic and Non-Neoplastic Lesions Arising in BK Virus/ tat Transgenic Mice
저자
by
Altavilla, Giuseppe
;
Trabanelli, Cecilia
;
Merlin, Michela
;
Caputo, Antonella
;
Lanfredi, Massimo
, et al.
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In
The American Journal of Pathology
1999 154(4):1231-1244
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7 . Academic Journal
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study.
저자
by
Neri, Marcella
;
Rossi, Rachele
;
Trabanelli, Cecilia
;
Mauro, Antonio
;
Selvatici, Rita
, et al.
소스
Frontiers in Genetics; 2020, p1-15, 15p
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7 .
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript
저자
by
Todeschini, Alice
;
Gualandi, Francesca
;
Trabanelli, Cecilia
;
Armaroli, Annarita
;
Ravani, Anna
, et al.
소스
In
Neuromuscular Disorders
October 2016 26(10):662-665
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7 . Academic Journal
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome.
저자
by
Gualandi, Francesca
;
Zaraket, Fatima
;
Malagù, Michele
;
Parmeggiani, Giulia
;
Trabanelli, Cecilia
, et al.
소스
Cardiology
. Jul2017, Vol. 137 Issue 4, p256-260. 5p. 1 Diagram, 1 Chart.
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7 . Academic Journal
Corrigendum to “MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region” [Brain Dev 2001; 23: S246–50]
저자
by
Vacca, Marcella
;
Filippini, Francesco
;
Budillon, Alberta
;
Rossi, Valeria
;
Ragione, Floriana Della
, et al.
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In
Brain and Development
November 2012 34(10):891-891
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7 . Academic Journal
Paternal germline mosaicism in collagen VI related myopathies.
저자
by
Armaroli, Annarita
;
Trabanelli, Cecilia
;
Scotton, Chiara
;
Venturoli, Anna
;
Selvatici, Rita
, et al.
소스
European Journal of Paediatric Neurology; Sep2015, Vol. 19 Issue 5, p533-536, 4p
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7 .
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study
저자
by
Marcella Neri
;
Rachele Rossi
;
Cecilia Trabanelli
;
Antonio Mauro
;
Rita Selvatici
, et al.
소스
Frontiers in Genetics, Vol 11 (2020)
Frontiers in Genetics
Open Access (OpenAIRE)
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7 . Academic Journal
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-Terminal domain: a case report.
저자
by
Martoni, Elena
;
Petrini, Stefania
;
Trabanelli, Cecilia
;
Sabatelli, Patrizia
;
Urciuolo, Anna
, et al.
소스
BMC Medical Genetics
. 2013, Vol. 14 Issue 1, p1-9. 9p. 3 Color Photographs, 2 Graphs.
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7 . Academic Journal
Exon skipping-mediated dystrophin reading frame restoration for small mutations.
저자
by
Spitali, Pietro
;
Rimessi, Paola
;
Fabris, Marina
;
Perrone, Daniela
;
Falzarano, Sofia
, et al.
소스
Human Mutation; Nov2009, Vol. 30 Issue 11, p1527-1534, 8p
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7 . Academic Journal
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies
저자
by
Armaroli, Annarita
;
Balla, Cristina
;
Trabanelli, Cecilia
;
Selvatici, Rita
;
Brieda, Alessandro
, et al.
소스
CIRCULATION-GENOMIC AND PRECISION MEDICINE
; APR 2020, 13 4, pe002751 3p.
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