Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing von Homma, Thais Kataoka, Freire, Bruna Lucheze, Honjo Kawahira, Rachel Sayuri, Dauber, Andrew, Funari, Mariana Ferreira de Assis, Lerario, Antônio Marcondes, Nishi, Mirian Yumie, Albuquerque, Edoarda Vasco de, Vasques, Gabriela de Andrade, Collett-Solberg, Paulo Ferrez, Miura Sugayama, Sofia Mizuho, Bertola, Debora Romeo, Kim, Chong Ae, Arnhold, Ivo Jorge Prado, Malaquias, Alexsandra Christianne, Jorge, Alexander Augusto de Lima

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Two Patients with Severe Short Stature due to a FBN1 Mutation (p.Ala1728Val) with a Mild Form of Acromicric Dysplasia von de Bruin, Christiaan, Finlayson, Courtney, Funari, Mariana F.A., Vasques, Gabriela A., Lucheze Freire, Bruna, Lerario, Antonio M., Andrew, Melissa, Hwa, Vivian, Dauber, Andrew, Jorge, Alexander A.L.

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Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature von Tolezano, Giovanna Cantini, Bastos, Giovanna Civitate, da Costa, Silvia Souza, Freire, Bruna Lucheze, Homma, Thais Kataoka, Honjo, Rachel Sayuri, Yamamoto, Guilherme Lopes, Passos-Bueno, Maria Rita, Koiffmann, Celia Priszkulnik, Kim, Chong Ae, Vianna-Morgante, Angela Maria, de Lima Jorge, Alexander Augusto, Bertola, Débora Romeo, Rosenberg, Carla, Krepischi, Ana Cristina Victorino

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Rare Causes and Differential Diagnosis in Patients With Silver-Russell Syndrome von Braga, Barbara Leitao, da Cunha Scalco, Renata, Homma, Thais Kataoka, Freire, Bruna Lucheze, Cellin, Laurana De Polli, Canton, Ana Pinheiro Machado, Lerario, Antônio Marcondes, de Assis Funari, Mariana Ferreira, de Souza, Vinicius, Bertola, Debora Romeo, Malaquias, Alexsandra Christianne, Mendonca, Berenice Bilharinho, de Lima Jorge, Alexander Augusto

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High frequency of genetic/epigenetic disorders in short stature children born with very low birth weight von Freire, Bruna Lucheze, Homma, Thais Kataoka, Lerario, Antônio Marcondes, Seo, Go Hun, Han, Heonjong, Assis Funari, Mariana Ferreira, Gomes, Nathalia Lisboa, Rosemberg, Carla, Krepischi, Ana Cristina Victorino, Andrade Vasques, Gabriela, Malaquias, Alexsandra Christianne, Lima Jorge, Alexander Augusto

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MON-333 Cutaneous Skeletal Hypophosphatemic Syndrome (Cshs) Caused by Somatic HRAS p.G13R Mutation: Long Follow-Up of Two Brazilian Women von Maia, Thamiris Freitas, Freire, Bruna Lucheze, Rodrigues, Andresa de Santi, Jorgetti, Vanda, Rocha, André Caroli, Moises, Caio Santiago, de Souza, Bruno Ferraz, Rodrigues, Marcelo Bordalo, Jorge, Alexander Augusto de Lima, Martin, Regina Matsunaga, Cabral, Hially R

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