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	1.	Associated anomalies in multi-malformed infants with cleft lip and palate: An epidemiologic study of nearly 6 million births in 23 EUROCAT registries. [electronic resource] by Calzolari, Elisa Pierini, Anna Astolfi, Gianni Bianchi, Fabrizio Neville, Amanda J Rivieri, Francesca Producer: 20070508 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Risk of congenital anomalies around a municipal solid waste incinerator: a GIS-based case-control study. [electronic resource] by Vinceti, Marco Malagoli, Carlotta Fabbi, Sara Teggi, Sergio Rodolfi, Rossella Garavelli, Livia Astolfi, Gianni Rivieri, Francesca Producer: 20090413 In: International journal of health geographics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype. [electronic resource] by Baroncini, Anna Rivieri, Francesca Capucci, Antonella Croci, Gianfranco Franchi, Fabrizia Sensi, Alberto Battaglia, Paola Aiello, Vincenzo Calzolari, Elisa Producer: 20060228 In: European journal of medical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Adverse pregnancy outcomes in a population exposed to the emissions of a municipal waste incinerator. [electronic resource] by Vinceti, Marco Malagoli, Carlotta Teggi, Sergio Fabbi, Sara Goldoni, Carlo De Girolamo, Gianfranco Ferrari, Paola Astolfi, Gianni Rivieri, Francesca Bergomi, Margherita Producer: 20090126 In: The Science of the total environment vol. 407 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Mutational screening of NOTCH3 gene reveals two novel mutations: complexity of CADASIL diagnosis. [electronic resource] by Mosca, Lorena Rivieri, Francesca Tanel, Raffaella Bonfante, Aldo Burlina, Alessandro Manfredini, Emanuela Primignani, Paola Gesu, Giovanni P Marocchi, Alessandro Penco, Silvana Producer: 20150814 In: Journal of molecular neuroscience : MN vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Familial Poland anomaly revisited. [electronic resource] by Baban, Anwar Torre, Michele Costanzo, Sara Gimelli, Stefania Bianca, Sebastiano Divizia, Maria Teresa Sénès, Filippo Maria Garavelli, Livia Rivieri, Francesca Lerone, Margherita Valle, Maura Ravazzolo, Roberto Calevo, Maria Grazia Producer: 20130620 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	De novo unbalanced translocations in Prader-Willi and Angelman syndrome might be the reciprocal product of inv dup(15)s. [electronic resource] by Rossi, Elena Giorda, Roberto Bonaglia, Maria Clara Candia, Stefania Di Grechi, Elena Franzese, Adriana Soli, Fiorenza Rivieri, Francesca Patricelli, Maria Grazia Saccilotto, Donatella Bonfante, Aldo Giglio, Sabrina Beri, Silvana Rocchi, Mariano Zuffardi, Orsetta Producer: 20121213 In: PloS one vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype. [electronic resource] by Nanetti, Lorenzo Sarto, Elisa Castaldo, Anna Magri, Stefania Mongelli, Alessia Rossi Sebastiano, Davide Canafoglia, Laura Grisoli, Marina Malaguti, Chiara Rivieri, Francesca D'Amico, Maria Chiara Di Bella, Daniela Franceschetti, Silvana Mariotti, Caterina Taroni, Franco Producer: 20190528 In: Journal of neurology vol. 266 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Syndromic intellectual disability: a new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant. [electronic resource] by Graziano, Claudio Wischmeijer, Anita Pippucci, Tommaso Fusco, Carlo Diquigiovanni, Chiara Nõukas, Margit Sauk, Martin Kurg, Ants Rivieri, Francesca Blau, Nenad Hoffmann, Georg F Chaubey, Alka Schwartz, Charles E Romeo, Giovanni Bonora, Elena Garavelli, Livia Seri, Marco Producer: 20150410 In: Gene vol. 559 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis. [electronic resource] by Palazzo, Viviana Provenzano, Aldesia Becherucci, Francesca Sansavini, Giulia Mazzinghi, Benedetta Orlandini, Valerio Giunti, Laura Roperto, Rosa Maria Pantaleo, Marilena Artuso, Rosangela Andreucci, Elena Bargiacchi, Sara Traficante, Giovanna Stagi, Stefano Murer, Luisa Benetti, Elisa Emma, Francesco Giordano, Mario Rivieri, Francesca Colussi, Giacomo Penco, Silvana Manfredini, Emanuela Caruso, Maria Rosa Garavelli, Livia Andrulli, Simeone Vergine, Gianluca Miglietti, Nunzia Mancini, Elena Malaventura, Cristina Percesepe, Antonio Grosso, Enrico Materassi, Marco Romagnani, Paola Giglio, Sabrina Producer: 20170926 In: Kidney international vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype. [electronic resource] by Cordelli, Duccio Maria Garavelli, Livia Savasta, Salvatore Guerra, Azzurra Pellicciari, Alessandro Giordano, Lucio Bonetti, Silvia Cecconi, Ilaria Wischmeijer, Anita Seri, Marco Rosato, Simonetta Gelmini, Chiara Della Giustina, Elvio Ferrari, Anna Rita Zanotta, Nicoletta Epifanio, Roberta Grioni, Daniele Malbora, Baris Mammi, Isabella Mari, Francesca Buoni, Sabrina Mostardini, Rosa Grosso, Salvatore Pantaleoni, Chiara Doz, Morena Poch-Olivé, Maria Luisa Rivieri, Francesca Sorge, Giovanni Simonte, Graziella Licata, Francesca Tarani, Luigi Terazzi, Emanuela Mazzanti, Laura Cerruti Mainardi, Paola Boni, Antonella Faravelli, Francesca Grasso, Marina Bianchi, Paolo Zollino, Marcella Franzoni, Emilio Producer: 20130701 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients. [electronic resource] by Garavelli, Livia Ivanovski, Ivan Caraffi, Stefano Giuseppe Santodirocco, Daniela Pollazzon, Marzia Cordelli, Duccio Maria Abdalla, Ebtesam Accorsi, Patrizia Adam, Margaret P Baldo, Chiara Bayat, Allan Belligni, Elga Bonvicini, Federico Breckpot, Jeroen Callewaert, Bert Cocchi, Guido Cuturilo, Goran Devriendt, Koenraad Dinulos, Mary Beth Djuric, Olivera Epifanio, Roberta Faravelli, Francesca Formisano, Debora Giordano, Lucio Grasso, Marina Grønborg, Sabine Iodice, Alessandro Iughetti, Lorenzo Lacombe, Didier Maggi, Massimo Malbora, Baris Mammi, Isabella Moutton, Sebastien Møller, Rikke Muschke, Petra Napoli, Manuela Pantaleoni, Chiara Pascarella, Rosario Pellicciari, Alessandro Poch-Olive, Maria Luisa Raviglione, Federico Rivieri, Francesca Russo, Carmela Savasta, Salvatore Scarano, Gioacchino Selicorni, Angelo Silengo, Margherita Sorge, Giovanni Tarani, Luigi Tone, Luis Gonzaga Toutain, Annick Trimouille, Aurelien Valera, Elvis Terci Vergano, Samantha Schrier Zanotta, Nicoletta Zollino, Marcella Dobyns, William B Paciorkowski, Alex R Producer: 20180213 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care. [electronic resource] by Ivanovski, Ivan Djuric, Olivera Caraffi, Stefano Giuseppe Santodirocco, Daniela Pollazzon, Marzia Rosato, Simonetta Cordelli, Duccio Maria Abdalla, Ebtesam Accorsi, Patrizia Adam, Margaret P Ajmone, Paola Francesca Badura-Stronka, Magdalena Baldo, Chiara Baldi, Maddalena Bayat, Allan Bigoni, Stefania Bonvicini, Federico Breckpot, Jeroen Callewaert, Bert Cocchi, Guido Cuturilo, Goran De Brasi, Daniele Devriendt, Koenraad Dinulos, Mary Beth Hjortshøj, Tina Duelund Epifanio, Roberta Faravelli, Francesca Fiumara, Agata Formisano, Debora Giordano, Lucio Grasso, Marina Grønborg, Sabine Iodice, Alessandro Iughetti, Lorenzo Kuburovic, Vladimir Kutkowska-Kazmierczak, Anna Lacombe, Didier Lo Rizzo, Caterina Luchetti, Anna Malbora, Baris Mammi, Isabella Mari, Francesca Montorsi, Giulia Moutton, Sebastien Møller, Rikke S Muschke, Petra Nielsen, Jens Erik Klint Obersztyn, Ewa Pantaleoni, Chiara Pellicciari, Alessandro Pisanti, Maria Antonietta Prpic, Igor Poch-Olive, Maria Luisa Raviglione, Federico Renieri, Alessandra Ricci, Emilia Rivieri, Francesca Santen, Gijs W Savasta, Salvatore Scarano, Gioacchino Schanze, Ina Selicorni, Angelo Silengo, Margherita Smigiel, Robert Spaccini, Luigina Sorge, Giovanni Szczaluba, Krzysztof Tarani, Luigi Tone, Luis Gonzaga Toutain, Annick Trimouille, Aurelien Valera, Elvis Terci Vergano, Samantha Schrier Zanotta, Nicoletta Zenker, Martin Conidi, Andrea Zollino, Marcella Rauch, Anita Zweier, Christiane Garavelli, Livia Producer: 20190201 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)