Defining the Critical Region for Intellectual Disability and Brain Malformations in 6q27 Microdeletions von Hanna, Marcela D., Moretti, Patricia N., P. de Oliveira, Claudiner, A. Rosa, Maria T., R. Versiani, Beatriz, de Oliveira, Silviene F., Pic-Taylor, Aline, F. Mazzeu, Juliana

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Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing von Soares de Lima, Yasmin, Chiabai, Marcela, Shen, Jun, Córdoba, Mara S., Versiani, Beatriz R., Benício, Rosenelle O.A., Pogue, Robert, Mingroni-Netto, Regina Célia, Lezirovitz, Karina, Pic-Taylor, Aline, Mazzeu, Juliana F., Oliveira, Silviene F.

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Genotype and phenotype correlation in a family with a 2q37 deletion downstream of HDAC4 von Moretti, Patricia N., Figueiredo, Ana Carolina V., Saliba, Aline, Versiani, Beatriz R., Oliveira, Silviene F., Pic‐Taylor, Aline, Mazzeu, Juliana F.

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Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review von de Souza, Vanessa Sodré, da Cunha, Gabriela Corassa Rodrigues, Versiani, Beatriz R., de Oliveira, Claudiner Pereira, Rosa, Maria Teresa Alves Silva, de Oliveira, Silviene F., Moretti, Patricia N., Mazzeu, Juliana F., Pic-Taylor, Aline

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Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome von Abreu, Ana Paula, Trarbach, Ericka Barbosa, de Castro, Margaret, Frade Costa, Elaine Maria, Versiani, Beatriz, Matias Baptista, Maria Tereza, Garmes, Heraldo Mendes, Mendonca, Berenice Bilharinho, Latronico, Ana Claudia

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Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of  KAL1 defects in patients with Kallmann syndrome von Montenegro, Luciana Ribeiro, Ph.D, Silveira, Leticia F.G., Ph.D, Tusset, Cintia, Ph.D, de Castro, Margaret, M.D., Ph.D, Versiani, Beatriz R., M.D., Ph.D, Latronico, Ana Claudia, M.D., Ph.D, Mendonca, Berenice Bilharinho, M.D., Ph.D, Trarbach, Ericka B., Ph.D

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ZDHHC9 X‐linked intellectual disability: Clinical and molecular characterization von Ramos, Anna Karolina Silva, Caldas‐Rosa, Erica Carine Campos, Ferreira, Bárbara Merfort, Versiani, Beatriz Ribeiro, Moretti, Patrícia Natalia, Oliveira, Silviene Fabiana, Pic‐Taylor, Aline, Mazzeu, Juliana F.

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Quantitative Magnetic Resonance Imaging Evaluation of the Olfactory System in Kallmann Syndrome: Correlation with a Clinical Smell Test von Koenigkam-Santos, Marcel, Santos, Antonio Carlos, Versiani, Beatriz R., Diniz, Paula Rejane B., Junior, Jorge Elias, de Castro, Margaret

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Partial 1q Duplications and Associated Phenotype von Morris, Marcos L.M., Baroneza, José E., Teixeira, Patricia, Medina, Cristina T.N., Cordoba, Mara S., Versiani, Beatriz R., Roese, Liege L., Freitas, Erika L., Fonseca, Ana C.S., dos Santos, Maria C.G., Pic-Taylor, Aline, Rosenberg, Carla, Oliveira, Silviene F., Ferrari, Iris, Mazzeu, Juliana F.

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Kallmann syndrome and mirror movements: White matter quantitative evaluation with magnetic resonance imaging von Koenigkam-Santos, Marcel, de Castro, Margaret, Versiani, Beatriz R, Diniz, Paula Rejane B, Santos, Antonio Carlos

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Morfologia urbana e apropriação social das praças de Brasília, Distrito Federal: da capital modernista à metrópole contemporânea von Silva Gomes, Patrícia, Versiani Ponce Lopes, Beatriz

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Kisspeptin (Kp-10) inhibits in vitro osteogenic differentiation of multipotent mesenchymal stromal cells extracted from the bone marrow of adult rats von Guimarães, Laís Bitencourt, Machado, Daniel Portela Dias, Carvalho Versiani Caldeira, Beatriz Ferreira, Vieira, Larissa Tiemi Matuzake, Santos, Gabriela Alves, Araújo, Fabiana Rocha, Machado, Leonardo Teotônio, Gomes, Dawidson Assis, Ocarino, Natália de Melo, Serakides, Rogéria, Reis, Amanda Maria Sena

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Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism von Versiani, Beatriz R., Trarbach, Ericka, Koenigkam-Santos, Marcel, Dos Santos, Antonio Carlos, Elias, Lucila L. K., Moreira, Ayrton C., Latronico, Ana Claudia, De Castro, Margaret

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Morfologia urbana e apropriação social das praças de Brasília, Distrito Federal: da capital modernista à metrópole contemporânea von Patrícia Silva Gomes, Beatriz Versiani Ponce Lopes

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Expanding the spectrum of TBL1XR1 deletion: Report of a patient with brain and cardiac malformations von Vaqueiro, Ana Carolina, de Oliveira, Claudiner Pereira, Cordoba, Mara Santos, Versiani, Beatriz Ribeiro, de Carvalho, Camila Xavier, Alves Rodrigues, Pedro Guilherme, de Oliveira, Silviene Fabiana, Mazzeu, Juliana Forte, Pic-Taylor, Aline

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SAT-299 48,xxyy Syndrome: A Case Report von Rodrigues, Stela LMR, Braz, Délia, Pfeilsticker, Alessandra, Versiani, Beatriz, Santarem de Oliveira, Renata, Lofrano-Porto, Adriana

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Novel Fibroblast Growth Factor Receptor 1 Mutations in Patients with Congenital Hypogonadotropic Hypogonadism with and without Anosmia von Trarbach, Ericka Barbosa, Costa, Elaine Maria Frade, Versiani, Beatriz, de Castro, Margaret, Baptista, Maria Tereza Matias, Garmes, Heraldo Mendes, de Mendonca, Berenice Bilharinho, Latronico, Ana Claudia

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Craniofacial and Dental Features in Kabuki Syndrome Patients von Sobral, Samantha Do Prado, Leite, André Ferreira, Figueiredo, Paulo Tadeu Sousa, Ferrari, Íris, Safatle, Heloísa Pires Neto, Córdoba, Mara Santos, Versiani, Beatriz Ribeiro, Acevedo, Ana Carolina, Mestrinho, Heliana Dantas

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Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes von Versiani, Beatriz Ribeiro, Gilbert-Barness, Enid, Giuliani, Liane Rosso, Peres, Luiz Cesar, Pina-Neto, João Monteiro

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ZDHHC9 X-linked intellectual disability: Clinical and molecular characterization von Ramos, Anna Karolina Silva, Caldas-Rosa, Erica Carine Campos, Ferreira, Bárbara Merfort, Versiani, Beatriz Ribeiro, Moretti, Patrícia Natalia, de Oliveira, Silviene Fabiana, Pic-Taylor, Aline, Mazzeu, Juliana F

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