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Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes.
Clin Genet. 2022 Jan;101(1):134-141. doi: 10.1111/cge.14072. Epub 2021 Nov 15.
Clin Genet. 2022.
PMID: 34664255
Genetic investigation of syndromic forms of obesity.
Carvalho LML, D'Angelo CS, Villela D, da Costa SS, de Lima Jorge AA, da Silva IT, de Oliveira Scliar M, Chaves LD, Krepischi ACV, Koiffmann CP, Rosenberg C.
Carvalho LML, et al. Among authors: de oliveira scliar m.
Int J Obes (Lond). 2022 Sep;46(9):1582-1586. doi: 10.1038/s41366-022-01149-5. Epub 2022 May 21.
Int J Obes (Lond). 2022.
PMID: 35597848
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DNA methylation patterns suggest the involvement of DNMT3B and TET1 in osteosarcoma development.
Pires SF, de Barros JS, da Costa SS, de Oliveira Scliar M, Van Helvoort Lengert A, Boldrini É, da Silva SRM, Tasic L, Vidal DO, Krepischi ACV, Maschietto M.
Pires SF, et al. Among authors: de oliveira scliar m.
Mol Genet Genomics. 2023 May;298(3):721-733. doi: 10.1007/s00438-023-02010-8. Epub 2023 Apr 5.
Mol Genet Genomics. 2023.
PMID: 37020053
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SCAF4-related syndromic intellectual disability.
Carvalho LML, Pinto CF, de Oliveira Scliar M, Otto PA, Krepischi ACV, Rosenberg C.
Carvalho LML, et al. Among authors: de oliveira scliar m.
Am J Med Genet A. 2023 Feb;191(2):570-574. doi: 10.1002/ajmg.a.63032. Epub 2022 Nov 5.
Am J Med Genet A. 2023.
PMID: 36333968
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