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DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients.
Urreizti R, Mayer K, Evrony GD, Said E, Castilla-Vallmanya L, Cody NAL, Plasencia G, Gelb BD, Grinberg D, Brinkmann U, Webb BD, Balcells S. Urreizti R, et al. Among authors: plasencia g. Eur J Hum Genet. 2020 Jan;28(1):64-75. doi: 10.1038/s41431-019-0374-9. Epub 2019 Mar 15. Eur J Hum Genet. 2020. PMID: 30877278 Free PMC article.
Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients.
Urreizti R, Mayer K, Evrony GD, Said E, Castilla-Vallmanya L, Cody NAL, Plasencia G, Gelb BD, Grinberg D, Brinkmann U, Webb BD, Balcells S. Urreizti R, et al. Among authors: plasencia g. Eur J Hum Genet. 2020 Jan;28(1):138. doi: 10.1038/s41431-019-0394-5. Eur J Hum Genet. 2020. PMID: 31477843 Free PMC article.
Promoting Latinx health equity through community-engaged policy and practice reforms in North Carolina.
Thoumi A, Plasencia G, Madanay F, Ho ES, Palmer C, Kaalund K, Chaudhry N, Labrador A, Rigsby K, Onunkwo A, Almonte I, Gonzalez-Guarda R, Martinez-Bianchi V, Cholera R. Thoumi A, et al. Among authors: plasencia g. Front Public Health. 2023 Nov 23;11:1227853. doi: 10.3389/fpubh.2023.1227853. eCollection 2023. Front Public Health. 2023. PMID: 38074704 Free PMC article.
44 results