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Caselli, Rossella
39
results:
Search for persons
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Online (39)
Mediatypes
Articles (Online) (18)
OpenAccess-fulltext (21)
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english (38)
italian (1)
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1
Myelodysplastic/Myeloproliferative Neoplasms with Features ..:
Bonometti, Arturo
;
Zanella, Simone
;
Rahal, Daoud
...
Hemato. 5 (2024) 3 - p. 230-250 , 2024
Link:
https://doi.org/10.3390/..
?
2
Testing single/combined clinical categories on 5110 Italian..:
Catusi, Ilaria
;
Recalcati, Maria Paola
;
Bestetti, Ilaria
...
Molecular Genetics & Genomic Medicine. 8 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1002/..
?
3
Low‐level TP53 mutational load antecedes clonal expansion i..:
Pinto, Anna Maria
;
Papa, Filomena T.
;
Frullanti, Elisa
...
British Journal of Haematology. 184 (2018) 4 - p. 657-659 , 2018
Link:
https://doi.org/10.1111/..
?
4
7p22.1 microduplication syndrome: Clinical and molecular ch..:
Caselli, Rossella
;
Ballarati, Lucia
;
Vignoli, Aglaia
...
European Journal of Medical Genetics. 58 (2015) 11 - p. 578-583 , 2015
Link:
https://doi.org/10.1016/..
?
5
Complex rearrangement involving 9p deletion and duplication..:
Recalcati, Maria Paola
;
Bellini, Melissa
;
Norsa, Lorenzo
...
Gene. 502 (2012) 1 - p. 40-45 , 2012
Link:
https://doi.org/10.1016/..
?
6
Deletion of the AP1S2 gene in a child with psychomotor dela..:
Ballarati, Lucia
;
Cereda, Anna
;
Caselli, Rossella
...
European Journal of Medical Genetics. 55 (2012) 2 - p. 124-127 , 2012
Link:
https://doi.org/10.1016/..
?
7
Electroclinical pattern in MECP2 duplication syndrome: Eigh..:
Vignoli, Aglaia
;
Borgatti, Renato
;
Peron, Angela
...
Epilepsia. 53 (2012) 7 - p. 1146-1155 , 2012
Link:
https://doi.org/10.1111/..
?
8
Genotype–phenotype correlations in a new case of 8p23.1 del..:
Ballarati, Lucia
;
Cereda, Anna
;
Caselli, Rossella
...
European Journal of Medical Genetics. 54 (2011) 1 - p. 55-59 , 2011
Link:
https://doi.org/10.1016/..
?
9
A 12.4 Mb duplication of 17q11.2q12 in a patient with psych..:
Caselli, Rossella
;
Ballarati, Lucia
;
Selicorni, Angelo
...
European Journal of Medical Genetics. 53 (2010) 5 - p. 325-328 , 2010
Link:
https://doi.org/10.1016/..
?
10
A 3 Mb deletion in 14q12 causes severe mental retardation, ..:
Papa, Filomena Tiziana
;
Mencarelli, Maria Antonietta
;
Caselli, Rossella
...
American Journal of Medical Genetics Part A. 146A (2008) 15 - p. 1994-1998 , 2008
Link:
https://doi.org/10.1002/..
?
11
Delineation of the phenotype associated with 7q36.1q36.2 de..:
Caselli, Rossella
;
Mencarelli, Maria Antonietta
;
Papa, Filomena Tiziana
...
American Journal of Medical Genetics Part A. 146A (2008) 9 - p. 1195-1199 , 2008
Link:
https://doi.org/10.1002/..
?
12
Private inherited microdeletion/microduplications: Implicat..:
Mencarelli, Maria Antonietta
;
Katzaki, Eleni
;
Papa, Filomena Tiziana
...
European Journal of Medical Genetics. 51 (2008) 5 - p. 409-416 , 2008
Link:
https://doi.org/10.1016/..
?
13
Clinical and molecular characterization of a patient with a..:
Mencarelli, Maria Antonietta
;
Caselli, Rossella
;
Pescucci, Chiara
...
American Journal of Medical Genetics Part A. 143A (2007) 8 - p. 858-865 , 2007
Link:
https://doi.org/10.1002/..
?
14
Autosomal recessive Alport syndrome: an in-depth clinical a..:
Longo, Ilaria
;
Scala, Elisa
;
Mari, Francesca
...
Nephrology Dialysis Transplantation. 21 (2005) 3 - p. 665-671 , 2005
Link:
https://doi.org/10.1093/..
?
15
CDKL5 belongs to the same molecular pathway of MeCP2 and it..:
Mari, Francesca
;
Azimonti, Sara
;
Bertani, Ilaria
...
Human Molecular Genetics. 14 (2005) 14 - p. 1935-1946 , 2005
Link:
https://doi.org/10.1093/..
1-15