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Genetics and Molecular Biology
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December 12, 2018
A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene
Fábio Tadeu Arrojo Martins, Berenice Dias Ramos, Edi Lúcia Sartorato
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Search research articles
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Showing results (1-10 of 1) with videos related to
Sort By:
Page
of 1
Genetics and Molecular Biology
|
December 12, 2018
A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene
Fábio Tadeu Arrojo Martins, Berenice Dias Ramos, Edi Lúcia Sartorato
Page
of 1