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Exome sequencing of 500 Brazilian patients with rare diseases: what we have learned.
Quaio, Caio Robledo D'Angioli Costa; Moreira, Caroline Monaco; Chung, Christine Hsiaoyun; Perazzio, Sandro Felix; Dutra, Aurelio Pimenta; Kim, Chong Ae.
Affiliation
  • Quaio CRDC; MD. Researcher and PhD Candidate, Instituto da Criança (ICr), Hospital das Clinicas HCFMUSP, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, BR.
  • Moreira CM; Medical Geneticist, Fleury Medicina e Saúde, São Paulo (SP), Brazil.
  • Chung CH; Medical Geneticist, Laboratório Clínico, Hospital Israelita Albert Einstein (HIAE), São Paulo (SP), Brazil.
  • Perazzio SF; MSc. Molecular Biology Leader, Fleury Medicina e Saúde, São Paulo (SP), Brazil.
  • Dutra AP; MD. Medical Geneticist, Fleury Medicina e Saúde, São Paulo (SP), Brazil.
  • Kim CA; MD, PhD. Immunology Division, Fleury Medicina e Saúde, São Paulo (SP), Brazil.
Sao Paulo Med J ; 140(5): 734-736, 2022.
Article in En | MEDLINE | ID: mdl-36102462
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rare Diseases / Exome Limits: Humans Country/Region as subject: America do sul / Brasil Language: En Journal: Sao Paulo Med J Journal subject: MEDICINA Year: 2022 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rare Diseases / Exome Limits: Humans Country/Region as subject: America do sul / Brasil Language: En Journal: Sao Paulo Med J Journal subject: MEDICINA Year: 2022 Document type: Article Affiliation country: Country of publication: