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Research Interests

Papers共 95 篇Author StatisticsCo-AuthorSimilar Experts

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Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome
Henrique Garcia Silveira,Carlos Eduardo Steiner, Giovana Toccoli, Luise Longo Angeloni, Julia Londero Heleno, Samira Spineli-Silva, Ana Mondadori dos Santos,Tarsis Paiva Vieira, Maria Isabel Melaragno,Vera Lucia Gil-da-Silva-Lopes
GENESno. 2 (2024): 211
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Microdeletion 1p32p31 Presenting with Moyamoya Disease and Incomplete Hippocampal Inversion
Ruy Pires de Oliveira-Sobrinho, Luciana Mota Bispo, Julia Londero Heleno, Fernanda Rocha Rojas Ayala, Fabiano Reis,Tarsis Paiva Vieira,Carlos Eduardo Steiner
MOLECULAR SYNDROMOLOGYno. 3 (2024): 225-231
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Microdeletion 3q13.2q21.2 in a Patient Previously Diagnosed with MOMO Syndrome
Ruy Pires de Oliveira-Sobrinho,Tarsis Paiva Vieira,Carlos Eduardo Steiner
MOLECULAR SYNDROMOLOGYpp.1-8, (2024)
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Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis
Ruy Pires de Oliveira-Sobrinho, Simone Appenzeller, Ianne Pessoa Holanda, Júlia Lôndero Heleno, Josep Jorente, On Behalf Of The Rare Genomes Project Consortium,Társis Paiva Vieira,Carlos Eduardo Steiner
Genesno. 4 (2024): 513
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