Goes C. Meira
Salvador, BA, Brazil
Last Updated: 09/26/2026
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Found 10 publications
Characterization of individuals with skeletal dysplasia at a referral center in Brazil.
Journal: Journal of community genetics
Published: January 13, 2026
Van der Woude syndrome and amniotic band sequence: A clue to a common genetic etiology? A case report.
Journal: Genetics and molecular biology
Published: June 24, 2024
ELMO2 biallelic pathogenic variants in a patient with gingival hypertrophy and cherubism phenotype: Case report and molecular review.
Journal: American journal of medical genetics. Part A
Published: January 27, 2024
Novel USP9X variant associated with syndromic intellectual disability in a female: A case study and review.
Journal: American journal of medical genetics. Part A
Published: April 01, 2020
Diagnosis of Atelosteogenesis Type I suggested by Fetal Ultrasonography and Atypical Paternal Phenotype with Mosaicism.
Journal: Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia
Published: September 20, 2018
Publisher Correction: Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells.
Journal: Nature communications
Published: March 15, 2018
Case of 15q26-qter deletion associated with a Prader-Willi phenotype.
Journal: European journal of medical genetics
Published: September 06, 2016
Genetics and management of the patient with orofacial cleft.
Journal: Plastic surgery international
Published: August 04, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026