Vieira Társis Paiva - Department of Medical Genetics, University of Campinas

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论文共 75 篇作者统计合作学者相似作者

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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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Prenatal findings in posnatal cases of disorders of sex development: experience from a tertiary specialized center in brazil

Kleber Andrade Cursino, Guilherme Mantelato Garcia,Beatriz Amstalden Barros,Tais Nitsch Mazzola,Helena Fabbri-Scallet,Mara Sanches Guaragna,Tarsis Antonio Paiva Vieira,Maricilda Palandi de Mello,Andrea Trevas Maciel-Guerra, Gil Guerra Jr

FETAL DIAGNOSIS AND THERAPYno. 1 (2024): 49-54

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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 SYNDROMOLOGY (2024)

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22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity

Melissa Bittencourt de Wallau, Ana Carolina Xavier,Carolina Araújo Moreno,Chong Ae Kim,Elaine Lustosa Mendes,Erlane Marques Ribeiro, Amanda Oliveira,Têmis Maria Félix, Agnes Cristina Fett-Conte, Luciana Cardoso Bonadia, Gabriela Roldão Correia-Costa,Isabella Lopes Monlleó,

Genes（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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SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism