Studi pubblicati nel 2007

  • Bernardini A, Capalbo A, D’Avanzo MG, Torrente I, Grammatico P, Dell’Edera D, Cavalcanti DP, Novelli A, Dalla piccola B. Five cases of supernumerary small ring chromosomes 1: heterogeneity and genotype-phenotype correlation. Eur J Med Genet. 2007 Mar-Apr;50(2):94-102. I.F.: 1,782
  • A. Borriello, A. Locasciulli, A.M. Bianco3, M. Criscuolo, V. Conti, P. Grammatico, S. Cappellacci, A Zatterale, F. Morgese, V. Cucciolla, D. Delia, F. Della Ragione, A. Savoia. A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia. Leukemia. 2007 Jan;21(1):72-78 I.F. 8,634   
  • Castori M, Silvestri E, Grammatico P, Dallapiccola B. A triploid fetus further expands etiological heterogenity in holoprosencephaly-diencephalic hamartoblastoma (HDH). Am J Med Genet A. 2007 Jun 15;143(12):1391-3. I.F.: 2,555
  • Castori M, Rinaldi R, Bianchi A, Caponetti A, Assumma M, Grammatico P. Pai syndromee: first patient with agenesis of the corpus callosum and literature review. Birth Defects Res A Clin Mol Teratol. 79 (10): 673-9, 2007. I.F.: 2,17
  • D’Elia AV, Pellizzari L, Fabbro D, Pianta A, Dovizia MT, Rinaldi R, Grammatico B, Grammatico P, Arduino C, Damante G A deletion 3' to the PAX6 gene in familial aniridia cases. Mol Vis. 2007 Jul 23;13:1245-50. I.F.: 2,464
  • Marrocco G, Bruner E, Vallasciani SA, Majore S, Grammatico P. do patients with hypospadias and cryptorchidism share a common phenotype? Case-control study of an Italian paediatric population. Journal of Pediatric Urology, 3,477-479,2007.