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2q24-q31 deletion: report of a case and review of the literature.
Pescucci C, Caselli R, Grosso S, Mencarelli MA, Mari F, Farnetani MA, Piccini B, Artuso R, Bruttini M, Priolo M, Zuffardi O, Gimelli S, Balestri P, Renieri A. Pescucci C, et al. Among authors: balestri p. Eur J Med Genet. 2007 Jan-Feb;50(1):21-32. doi: 10.1016/j.ejmg.2006.09.001. Epub 2006 Sep 17. Eur J Med Genet. 2007. PMID: 17088112 Review.
Private inherited microdeletion/microduplications: implications in clinical practice.
Mencarelli MA, Katzaki E, Papa FT, Sampieri K, Caselli R, Uliana V, Pollazzon M, Canitano R, Mostardini R, Grosso S, Longo I, Ariani F, Meloni I, Hayek J, Balestri P, Mari F, Renieri A. Mencarelli MA, et al. Among authors: balestri p. Eur J Med Genet. 2008 Sep-Oct;51(5):409-16. doi: 10.1016/j.ejmg.2008.06.003. Epub 2008 Jul 9. Eur J Med Genet. 2008. PMID: 18657637
Chromosome 18 aberrations and epilepsy: a review.
Grosso S, Pucci L, Di Bartolo RM, Gobbi G, Bartalini G, Anichini C, Scarinci R, Balestri M, Farnetani MA, Cioni M, Morgese G, Balestri P. Grosso S, et al. Among authors: balestri p, balestri m. Am J Med Genet A. 2005 Apr 1;134A(1):88-94. doi: 10.1002/ajmg.a.30575. Am J Med Genet A. 2005. PMID: 15690352
Medial temporal lobe dysgenesis in Muenke syndrome and hypochondroplasia.
Grosso S, Farnetani MA, Berardi R, Bartalini G, Carpentieri M, Galluzzi P, Mostardini R, Morgese G, Balestri P. Grosso S, et al. Among authors: balestri p. Am J Med Genet A. 2003 Jul 1;120A(1):88-91. doi: 10.1002/ajmg.a.10171. Am J Med Genet A. 2003. PMID: 12794698
Craniofacial dyssynostosis: case report and review.
Grosso S, Vivarelli R, Muraca MC, Berardi R, Marconcini S, Morgese G, Balestri P. Grosso S, et al. Among authors: balestri p. Am J Med Genet A. 2004 Sep 1;129A(3):300-2. doi: 10.1002/ajmg.a.30186. Am J Med Genet A. 2004. PMID: 15326632
178 results