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

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Bibliographic Details
Date:2022
Main Authors: L. V. Popovych, A. V. Shatillo, N. B. Zelinska, L. V. Tavokina, O. V. Horodna, H. B. Livshyts, D. A. Sirokha, L. A. Livshyts
Format: Article
Language:English
Published: 2022
Series:Cytology and genetics
Online Access:http://jnas.nbuv.gov.ua/article/UJRN-0001365905
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Journal Title:Library portal of National Academy of Sciences of Ukraine | LibNAS

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Library portal of National Academy of Sciences of Ukraine | LibNAS