Molecular diagnosis of Chinese patients with 21-hydroxylase deficiency and analysis of genotypeaephenotype correlations
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Target Article[edit | edit source]
Molecular diagnosis of Chinese patients with 21-hydroxylase deficiency and analysis of genotypeaephenotype correlations; B Zhang, L Lu, Z Lu; 2017; doi_citing_unknown
Retraction[edit | edit source]
Bilateral ovarian steroid cell tumor in congenital adrenal hyperplasia due to classic 11ß-hydroxylase deficiency ; Firdevs Bas Nucin Saka Feyza Darendeliler Siki Tuzlah Ridvan Ilhan Ruveyde Bundak Hulya Gonuz; 06/01/2000
Citation piece[edit | edit source]
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