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

• Дата: 2022
• Автори: L. V. Popovych, A. V. Shatillo, N. B. Zelinska, L. V. Tavokina, O. V. Horodna, H. B. Livshyts, D. A. Sirokha, L. A. Livshyts
• Формат: Стаття
• Мова: English
• Опубліковано: 2022
• Назва видання: Cytology and genetics
• Онлайн доступ: http://jnas.nbuv.gov.ua/article/UJRN-0001365905
• Назва журналу: Library portal of National Academy of Sciences of Ukraine | LibNAS