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	1.	Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers. [electronic resource] by Vainzof, Mariz Feitosa, Leticia Canovas, Marta Ayub-Guerrieri, Danielle Pavanello, Rita de Cássia M Zatz, Mayana Producer: 20161214 In: Neuromuscular disorders : NMD vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Assessing pathogenicity for novel mutation/sequence variants: the value of healthy older individuals. [electronic resource] by Zatz, Mayana Pavanello, Rita de Cassia M Lourenço, Naila Cristina V Cerqueira, Antonia Lazar, Monize Vainzof, Mariz Producer: 20130507 In: Neuromolecular medicine vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2. [electronic resource] by Passos-Bueno, Maria Rita Armelin, Lucia Maria Alonso, Luís Garcia Neustein, Isaac Sertié, Andréa L Abe, Kikue Pavanello, Rita de Cássia Elkis, Lívia C Koiffmann, Célia P Producer: 20030407 In: American journal of medical genetics vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome. [electronic resource] by Mazzeu, Juliana F Krepischi-Santos, Ana Cristina Rosenberg, Carla Szuhai, Karoly Knijnenburg, Jeroen Weiss, Janneke M M Kerkis, Irina Mustacchi, Zan Colin, Guilherme Mombach, Rômulo Pavanello, Rita de Cássia M Otto, Paulo A Vianna-Morgante, Angela M Producer: 20080116 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)