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Three cases with de novo 6q imbalance and variable prenatal phenotype.
Grati FR, Lalatta F, Turolla L, Cavallari U, Gentilin B, Rossella F, Cetin I, Antonazzo P, Bellotti M, Dulcetti F, Baldo D, Tenconi R, Simoni G, Miozzo M. Grati FR, et al. Among authors: gentilin b. Am J Med Genet A. 2005 Jul 30;136(3):254-8. doi: 10.1002/ajmg.a.30837. Am J Med Genet A. 2005. PMID: 15957159
SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome.
Gervasini C, Grati FR, Lalatta F, Tabano S, Gentilin B, Colapietro P, De Toffol S, Frontino G, Motta F, Maitz S, Bernardini L, Dallapiccola B, Fedele L, Larizza L, Miozzo M. Gervasini C, et al. Among authors: gentilin b. Genet Med. 2010 Oct;12(10):634-40. doi: 10.1097/GIM.0b013e3181ed6185. Genet Med. 2010. PMID: 20847698 Free article.
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: gentilin b. 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
Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior.
Lalatta F, Folliero E, Cavallari U, Di Segni M, Gentilin B, Fogliani R, Quagliarini D, Vizziello P, Monti F, Gargantini L. Lalatta F, et al. Among authors: gentilin b. Ital J Pediatr. 2012 Oct 3;38:52. doi: 10.1186/1824-7288-38-52. Ital J Pediatr. 2012. PMID: 23034220 Free PMC article.
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
Calvello M, Tabano S, Colapietro P, Maitz S, Pansa A, Augello C, Lalatta F, Gentilin B, Spreafico F, Calzari L, Perotti D, Larizza L, Russo S, Selicorni A, Sirchia SM, Miozzo M. Calvello M, et al. Among authors: gentilin b. Epigenetics. 2013 Oct;8(10):1053-60. doi: 10.4161/epi.25812. Epub 2013 Aug 5. Epigenetics. 2013. PMID: 23917791 Free PMC article.
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
Fontana L, Gentilin B, Fedele L, Gervasini C, Miozzo M. Fontana L, et al. Among authors: gentilin b. Clin Genet. 2017 Feb;91(2):233-246. doi: 10.1111/cge.12883. Epub 2016 Nov 16. Clin Genet. 2017. PMID: 27716927 Review.
Dysmorphologic assessment in 115 Mayer-Rokitansky-Küster-Hauser patients.
Lalatta F, Motta F, Restelli E, Bellini M, Miozzo M, Gervasini C, Dallapiccola B, Gentilin B, Fedele L. Lalatta F, et al. Among authors: gentilin b. Clin Dysmorphol. 2015 Jul;24(3):95-101. doi: 10.1097/MCD.0000000000000087. Clin Dysmorphol. 2015. PMID: 25968587
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