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	1.	Vertical transmission of a frontonasal phenotype caused by a novel ALX4 mutation. [electronic resource] by Bertola, Débora R Rodrigues, Melina G Quaio, Caio R D C Kim, Chong A Passos-Bueno, Maria Rita Producer: 20130805 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)
	2.	Autoimmune disease and multiple autoantibodies in 42 patients with RASopathies. [electronic resource] by Quaio, Caio R D C Carvalho, Jozélio F da Silva, Clovis A Bueno, Cleonice Brasil, Amanda S Pereira, Alexandre C Jorge, Alexander A L Malaquias, Alexsandra C Kim, Chong A Bertola, Débora R Producer: 20121026 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)
	3.	Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features. [electronic resource] by Stankiewicz, Paweł Khan, Tahir N Szafranski, Przemyslaw Slattery, Leah Streff, Haley Vetrini, Francesco Bernstein, Jonathan A Brown, Chester W Rosenfeld, Jill A Rednam, Surya Scollon, Sarah Bergstrom, Katie L Parsons, Donald W Plon, Sharon E Vieira, Marta W Quaio, Caio R D C Baratela, Wagner A R Acosta Guio, Johanna C Armstrong, Ruth Mehta, Sarju G Rump, Patrick Pfundt, Rolph Lewandowski, Raymond Fernandes, Erica M Shinde, Deepali N Tang, Sha Hoyer, Juliane Zweier, Christiane Reis, André Bacino, Carlos A Xiao, Rui Breman, Amy M Smith, Janice L Katsanis, Nicholas Bostwick, Bret Popp, Bernt Davis, Erica E Yang, Yaping Producer: 20171016 In: American journal of human genetics vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)