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Prague Medical Report|December 20, 2012
Cryptic chromosome rearrangements in five patients, with normal and/or abnormal karyotypes, associated with mental retardation, autism and/or epilepsy, detected by BAC genome array-CGHV Cabras, A Milia, C Montaldo, et al.
Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Partial proximal trisomy 10q syndrome: a new caseA Nucaro, A Faedda, A Cao, et al.
Prenatal Diagnosis|October 1, 1988
Pseudomosaic centric fission of chromosome 4 in amniotic cellsA Nucaro, A M Falchi, G Monni, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Duplication of the terminal band of the long arm of chromosome 7: a new caseL Boccone, D Gasperini, G Pilloni, et al.
Genetic Counseling (Geneva, Switzerland)|June 21, 2008
A family with segregation of an unbalanced translocation (7;13) (q36;q32) in three patients with severe mental retardation, microcephaly and dysmorphic features, detected by subtelomere FISH: genetic counselling and prenatal diagnosisA Nucaro, G Crisponi, L Minafra, et al.
Minerva Stomatologica|October 14, 2010
A rapid sample method for HLA haplotype typization. A preliminary study on celiac patientsM Erriu, F Boscarelli, C Peluffo, et al.
American Journal of Medical Genetics|April 1, 1992
X-linked mental retardation and characteristic physical features in two brothers with duplication Xp22-XpterC Cianchetti, F Muntoni, A M Falchi, et al.
Helvetica Paediatrica Acta|August 1, 1983
Methyl-prednisolone treatment of serum HBsAg negative chronic active hepatitis occurring in transfusion-dependent thalassemia majorS De Virgiliis, F Argiolu, M Rais, et al.
The American Journal of Pediatric Hematology/Oncology|January 1, 1983
Effect of subcutaneous desferrioxamine on iron balance in young thalassemia major patientsS De Virgiliis, P Cossu, C Toccafondi, et al.
Acta Haematologica|January 1, 1982
Iron chelation in transfusion-dependent thalassemia with chronic hepatitisS De Virgiliis, P Cossu, G Sanna, et al.
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