Caselli, Rossella
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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
 
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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
 
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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
 
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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
 
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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
 
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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
 
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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
 
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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
 
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