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Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients.
Eur J Med Genet. 2007 Sep-Oct;50(5):327-37. doi: 10.1016/j.ejmg.2007.05.005. Epub 2007 Jun 6.
Eur J Med Genet. 2007.
PMID: 17625998
An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.
Ferrero GB, Howald C, Micale L, Biamino E, Augello B, Fusco C, Turturo MG, Forzano S, Reymond A, Merla G.
Ferrero GB, et al. Among authors: forzano s.
Eur J Hum Genet. 2010 Jan;18(1):33-8. doi: 10.1038/ejhg.2009.108.
Eur J Hum Genet. 2010.
PMID: 19568270
Free PMC article.
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Prenatal features of Noonan syndrome: prevalence and prognostic value.
Baldassarre G, Mussa A, Dotta A, Banaudi E, Forzano S, Marinosci A, Rossi C, Tartaglia M, Silengo M, Ferrero GB.
Baldassarre G, et al. Among authors: forzano s.
Prenat Diagn. 2011 Oct;31(10):949-54. doi: 10.1002/pd.2804. Epub 2011 Jul 11.
Prenat Diagn. 2011.
PMID: 21744363
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Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis.
Lalatta F, Quagliarini D, Folliero E, Cavallari U, Gentilin B, Castorina P, Forzano F, Forzano S, Grosso E, Viassolo V, Naretto VG, Gattone S, Ceriani F, Faravelli F, Gargantini L.
Lalatta F, et al. Among authors: forzano s.
Eur J Pediatr. 2010 Oct;169(10):1255-61. doi: 10.1007/s00431-010-1221-8. Epub 2010 May 15.
Eur J Pediatr. 2010.
PMID: 20473517
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