Popovych, L. V., Shatillo, A. V., Zelinska, N. B., Tavokina, L. V., Horodna, O. V., Livshyts, H. B., . . . Livshyts, L. A. (2022). 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 and neuromuscular pathology.
Chicago Style (17th ed.) CitationPopovych, L. V., A. V. Shatillo, N. B. Zelinska, L. V. Tavokina, O. V. Horodna, H. B. Livshyts, D. A. Sirokha, and L. A. Livshyts. 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 and Neuromuscular Pathology. 2022.
MLA (8th ed.) CitationPopovych, L. V., et al. 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 and Neuromuscular Pathology. 2022.