The Combination of Chromosomal Reorganization and Inherited Point Mutation Has Led to the Development of a Rare Clinical Phenotype in a Patient with Disorder of Sex Differentiation... von Popovych, L. V., Shatillo, A. V., Zelinska, N. B., Tavokina, L. V., Gorodna, O. V., Livshits, G. B., Sirokha, D. A., Livshits, L. A.

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Supplementary Material for: Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis von D., Sirokha, A., Rayevsky, O., Gorodna, V., Kalynovskyi, N., Zelinska, O., Samson, K., Kwiatkowska, S., Nef, J., Jaruzelska, K., Kusz-Zamelczyk, L., Livshits

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