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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 1 |
2022 | 2 |
2024 | 2 |
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Page 1
Congenital limb deficiency: Genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms.
Clin Genet. 2021 Nov;100(5):615-623. doi: 10.1111/cge.14041. Epub 2021 Aug 9.
Clin Genet. 2021.
PMID: 34341987
Vertebral segmentation defects in a Brazilian cohort: Clinical and molecular analysis focused on spondylocostal dysostosis.
Linnenkamp B, Girardi R, Rocha L, Yamamoto G, Ceroni JR, Mendes AEC, Honjo R, Oliveira LA, Amemiya RB, Quaio C, de Oliveira Filho JB, Kim CA, Bertola D.
Linnenkamp B, et al.
Clin Genet. 2022 Apr;101(4):476-478. doi: 10.1111/cge.14118. Epub 2022 Feb 9.
Clin Genet. 2022.
PMID: 35137400
No abstract available.
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Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature.
Tolezano GC, Bastos GC, da Costa SS, Freire BL, Homma TK, Honjo RS, Yamamoto GL, Passos-Bueno MR, Koiffmann CP, Kim CA, Vianna-Morgante AM, de Lima Jorge AA, Bertola DR, Rosenberg C, Krepischi ACV.
Tolezano GC, et al.
J Autism Dev Disord. 2024 Mar;54(3):1181-1212. doi: 10.1007/s10803-022-05853-z. Epub 2022 Dec 11.
J Autism Dev Disord. 2024.
PMID: 36502452
Review.
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Clinical Characterization and Underlying Genetic Findings in Brazilian Patients with Syndromic Microcephaly Associated with Neurodevelopmental Disorders.
Tolezano GC, Bastos GC, da Costa SS, Scliar MO, de Souza CFM, Van Der Linden H Jr, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AAL, Bertola DR, Krepischi ACV.
Tolezano GC, et al.
Mol Neurobiol. 2024 Jan 5. doi: 10.1007/s12035-023-03894-8. Online ahead of print.
Mol Neurobiol. 2024.
PMID: 38180615
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