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Expanding the Phenotype of 8p23.1 Deletion Syndrome: Eight New Cases Resembling the Clinical Spectrum of 22q11.2 Microdeletion.
Montenegro MM, Camilotti D, Quaio CRDC, Gasparini Y, Zanardo ÉA, Rangel-Santos A, Novo-Filho GM, Francisco G, Liro L, Nascimento A, Chehimi SN, Soares DCQ, Krepischi ACV, Grassi MS, Honjo RS, Palmeira P, Kim CA, Carneiro-Sampaio MMS, Rosenberg C, Kulikowski LD. Montenegro MM, et al. Among authors: soares dcq. J Pediatr. 2023 Jan;252:56-60.e2. doi: 10.1016/j.jpeds.2022.08.051. Epub 2022 Sep 5. J Pediatr. 2023. PMID: 36067875
Terminal deletion 6p23: a case report.
Kormann-Bortolotto MH, Farah LM, Soares D, Corbani M, Müller R, Adell AC. Kormann-Bortolotto MH, et al. Am J Med Genet. 1990 Dec;37(4):475-7. doi: 10.1002/ajmg.1320370410. Am J Med Genet. 1990. PMID: 2260591
Prevalence and clinical implications of germline pathogenic variants in cancer predisposing genes in young patients across sarcoma subtypes.
Carvalho NA, Santiago KM, Maia JML, Costa FD, Formiga MN, Soares DCQ, Paixão D, Mello CAL, Costa CMLD, Rocha JCCD, Rivera B, Carraro DM, Torrezan GT. Carvalho NA, et al. Among authors: soares dcq. J Med Genet. 2023 Dec 21;61(1):61-68. doi: 10.1136/jmg-2023-109269. J Med Genet. 2023. PMID: 37536918 Free PMC article.
Natural history of 39 patients with Achondroplasia.
Ceroni JRM, Soares DCQ, Testai LC, Kawahira RSH, Yamamoto GL, Sugayama SMM, Oliveira LAN, Bertola DR, Kim CA. Ceroni JRM, et al. Among authors: soares dcq. Clinics (Sao Paulo). 2018 Jul 2;73:e324. doi: 10.6061/clinics/2018/e324. Clinics (Sao Paulo). 2018. PMID: 29972438 Free PMC article.