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Tarsis Paiva Vieira

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Professor

University of Campinas

Brazil

Research Interests

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Professors in Medical Science

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Genomic imbalances in patients with clinical suspicion of 22q11.2 Deletion Syndrome

Open Date: 2014-12-01

Close Date: 2017-11-01

Articles (15)

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Collaborators (7)

Miikka Vikkula

Full Professor of Human Genetics

Université catholique de Louvain

BELGIUM

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Sofia Helena Valente Lemos-Marini

Professora Assistente

University of Campinas

BRAZIL

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André Morcillo

Professor

University of Campinas

BRAZIL

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Antonia Marques-de-Faria

Associate Professor

University of Campinas

BRAZIL

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Marcio Miranda

Professor

University of Campinas

BRAZIL

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Tiago Henrique de Souza

Médico Assistente

University of Campinas

BRAZIL

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Maricilda Palandi de Mello

Professor

University of Campinas

BRAZIL

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Tarsis Paiva Vieira

Research Interests

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Recent Grants

Articles (15)

First Report of Uniparental Isodisomy of Chromosome 15 Revealing Angelman Syndrome and Microphthalmia Associated With a Novel Homozygous ALDH1A3 Variant

Whole-genome sequencing in Brazilian patients with neurofibromatosis type 1, including novel variants, incidental findings, and dual diagnoses

Whole exome sequencing in 18 Brazilian families with vertical transmission of non-syndromic oral clefts

Can Individuals with 47,XYY Karyotypes Exist without Male Phenotype? A Narrative Literature Review and Case Report

Growth charts of Brazilian girls with Turner syndrome without the use of GH or oxandrolone

SMAD4 Pathogenic Variants in Seven New Brazilian Individuals With Myhre Syndrome Including a New Family

Molecular investigation in individuals with orofacial clefts and microphthalmia-anophthalmia-coloboma spectrum

Patients with genital ambiguity referred without a sex definition: the relationship between clinical picture and defined sex of rearing

Overlapping Spectrum of Craniofacial Microsomia Phenotype in Cat-Eye Syndrome

Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis

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

Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome

SATB2-Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review

Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study

Rare 15q21.1q22.31 Duplication Due to a Familial Chromosomal Insertion and Diagnostic Investigation in a Carrier of Balanced Chromosomal Rearrangement and Intellectual Disability

Collaborators (7)

Miikka Vikkula

Sofia Helena Valente Lemos-Marini

André Morcillo

Antonia Marques-de-Faria

Marcio Miranda

Tiago Henrique de Souza

Maricilda Palandi de Mello

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