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Dive into the research topics of 'Difficulties in diagnosis and treatment of 5α-reductase type 2 deficiency in a newborn with 46,XY DSD'. Together they form a unique fingerprint.- Sort by
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Kerstin N. Walter, Frederike B. Kienzle, Alexander Frankenschmidt, Olaf Hiort, Stefan A. Wudy, Natascha Van Der Werf-Grohmann, Andrea Superti-Furga, Karl Otfried Schwab