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	1.	Areal bone mineral density in children and adolescents with Marfan syndrome: evidence of an evolving problem. [electronic resource] by Trifirò, Giuliana Marelli, Susan Viecca, Maurizio Mora, Stefano Pini, Alessandro Producer: 20151208 In: Bone vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Bilateral frontoparietal polymicrogyria (BFPP) syndrome secondary to a 16q12.1-q21 chromosome deletion involving GPR56 gene. [electronic resource] by Borgatti, Renato Marelli, Susan Bernardini, Laura Novelli, Antonio Cavallini, Anna Tonelli, Alessandra Bassi, Maria Teresa Dallapiccola, Bruno Producer: 20100217 In: Clinical genetics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Subtelomeric trisomy 21q: a new benign chromosomal variant. [electronic resource] by Bonaglia, Maria Clara Marelli, Susan Gottardi, Giulietta Zucca, Claudio Pramparo, Tiziano Giorda, Roberto Grasso, Rita Borgatti, Renato Zuffardi, Orsetta Producer: 20070322 In: European journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus Callosum. [electronic resource] by Romaniello, Romina Marelli, Susan Giorda, Roberto Bedeschi, Maria F Bonaglia, Maria C Arrigoni, Filippo Triulzi, Fabio Bassi, Maria T Borgatti, Renato Producer: 20180105 In: Journal of child neurology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Pharmacogenetic approach to losartan in Marfan patients: a starting point to improve dosing regimen? [electronic resource] by Falvella, Felicia Stefania Marelli, Susan Cheli, Stefania Montanelli, Stefano Viecca, Federico Salvi, Lucia Ferrara, Alfio Clementi, Emilio Trifirò, Giuliana Pini, Alessandro Producer: 20171110 In: Drug metabolism and personalized therapy vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype. [electronic resource] by Bonaglia, Maria Clara Ciccone, Roberto Gimelli, Giorgio Gimelli, Stefania Marelli, Susan Verheij, Joke Giorda, Roberto Grasso, Rita Borgatti, Renato Pagone, Filomena Rodrìguez, Laura Martinez-Frias, Maria-Luisa van Ravenswaaij, Conny Zuffardi, Orsetta Producer: 20090107 In: European journal of human genetics : EJHG vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletions. [electronic resource] by Bonaglia, Maria C Marelli, Susan Novara, Francesca Commodaro, Simona Borgatti, Renato Minardo, Grazia Memo, Luigi Mangold, Elisabeth Beri, Silvana Zucca, Claudio Brambilla, Daniele Molteni, Massimo Giorda, Roberto Weber, Ruthild G Zuffardi, Orsetta Producer: 20110228 In: European journal of human genetics : EJHG vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and females. [electronic resource] by Giorda, Roberto Bonaglia, M Clara Beri, Silvana Fichera, Marco Novara, Francesca Magini, Pamela Urquhart, Jill Sharkey, Freddie H Zucca, Claudio Grasso, Rita Marelli, Susan Castiglia, Lucia Di Benedetto, Daniela Musumeci, Sebastiano A Vitello, Girolamo A Failla, Pinella Reitano, Santina Avola, Emanuela Bisulli, Francesca Tinuper, Paolo Mastrangelo, Massimo Fiocchi, Isabella Spaccini, Luigina Torniero, Claudia Fontana, Elena Lynch, Sally Ann Clayton-Smith, Jill Black, Graeme Jonveaux, Philippe Leheup, Bruno Seri, Marco Romano, Corrado dalla Bernardina, Bernardo Zuffardi, Orsetta Producer: 20090930 In: American journal of human genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome. [electronic resource] by Bonaglia, Maria Clara Giorda, Roberto Beri, Silvana De Agostini, Cristina Novara, Francesca Fichera, Marco Grillo, Lucia Galesi, Ornella Vetro, Annalisa Ciccone, Roberto Bonati, Maria Teresa Giglio, Sabrina Guerrini, Renzo Osimani, Sara Marelli, Susan Zucca, Claudio Grasso, Rita Borgatti, Renato Mani, Elisa Motta, Cristina Molteni, Massimo Romano, Corrado Greco, Donatella Reitano, Santina Baroncini, Anna Lapi, Elisabetta Cecconi, Antonella Arrigo, Giulia Patricelli, Maria Grazia Pantaleoni, Chiara D'Arrigo, Stefano Riva, Daria Sciacca, Francesca Dalla Bernardina, Bernardo Zoccante, Leonardo Darra, Francesca Termine, Cristiano Maserati, Emanuela Bigoni, Stefania Priolo, Emanuela Bottani, Armand Gimelli, Stefania Bena, Frederique Brusco, Alfredo di Gregorio, Eleonora Bagnasco, Irene Giussani, Ursula Nitsch, Lucio Politi, Pierluigi Martinez-Frias, Maria Luisa Martínez-Fernández, Maria Luisa Martínez Guardia, Nieves Bremer, Anna Anderlid, Britt-Marie Zuffardi, Orsetta Producer: 20120221 In: PLoS genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)