Microdeletion 1p32p31 Presenting with Moyamoya Disease and Incomplete Hippocampal Inversion von Pires de Oliveira-Sobrinho, Ruy, Bispo, Luciana Mota, Heleno, Julia Lôndero, Rojas Ayala, Fernanda Rocha, Reis, Fabiano, Vieira, Társis Paiva, Steiner, Carlos Eduardo

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Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis von de Oliveira-Sobrinho, Ruy Pires, Appenzeller, Simone, Holanda, Ianne Pessoa, Heleno, Júlia Lôndero, Jorente, Josep, On Behalf Of The Rare Genomes Project Consortium, Vieira, Társis Paiva, Steiner, Carlos Eduardo

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Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome von Silveira, Henrique Garcia, Steiner, Carlos Eduardo, Toccoli, Giovana, Angeloni, Luise Longo, Heleno, Júlia Lôndero, Spineli-Silva, Samira, Dos Santos, Ana Mondadori, Vieira, Társis Paiva, Melaragno, Maria Isabel, Gil-da-Silva-Lopes, Vera Lúcia

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Variants in IKMT2A/I in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome von Silveira, Henrique Garcia, Steiner, Carlos Eduardo, Toccoli, Giovana, Angeloni, Luise Longo, Heleno, Júlia Lôndero, Spineli-Silva, Samira, dos Santos, Ana Mondadori, Vieira, Társis Paiva, Melaragno, Maria Isabel, Gil-da-Silva-Lopes, Vera Lúcia

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Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis von de Oliveira-Sobrinho, Ruy Pires, Appenzeller, Simone, Holanda, Ianne Pessoa, Heleno, Júlia Lôndero, Jorente, Josep, Vieira, Társis Paiva, Steiner, Carlos Eduardo

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