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- Q90389391 description "article scientifique publié en 2018" @default.
- Q90389391 description "artículu científicu espublizáu n'ochobre de 2018" @default.
- Q90389391 description "im Oktober 2018 veröffentlichter wissenschaftlicher Artikel" @default.
- Q90389391 description "scientific article published on 01 October 2018" @default.
- Q90389391 description "wetenschappelijk artikel" @default.
- Q90389391 description "наукова стаття, опублікована в жовтні 2018" @default.
- Q90389391 name "A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene" @default.
- Q90389391 name "A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene" @default.
- Q90389391 type Item @default.
- Q90389391 label "A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene" @default.
- Q90389391 label "A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene" @default.
- Q90389391 prefLabel "A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene" @default.
- Q90389391 prefLabel "A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene" @default.
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- Q90389391 P1476 "A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene" @default.
- Q90389391 P2093 "Berenice Dias Ramos" @default.
- Q90389391 P2093 "Edi Lúcia Sartorato" @default.
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- Q90389391 P356 "10.1590/1678-4685-GMB-2017-0194" @default.
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