Vasilyeva, T.A.; Marakhonov, A.V.; Sukhanova, N.V.; Kutsev, S.I.; Zinchenko, R.A.
Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome. Genes 2020, 11, 812.
https://doi.org/10.3390/genes11070812
AMA Style
Vasilyeva TA, Marakhonov AV, Sukhanova NV, Kutsev SI, Zinchenko RA.
Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome. Genes. 2020; 11(7):812.
https://doi.org/10.3390/genes11070812
Chicago/Turabian Style
Vasilyeva, Tatyana A., Andrey V. Marakhonov, Natella V. Sukhanova, Sergey I. Kutsev, and Rena A. Zinchenko.
2020. "Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome" Genes 11, no. 7: 812.
https://doi.org/10.3390/genes11070812
APA Style
Vasilyeva, T. A., Marakhonov, A. V., Sukhanova, N. V., Kutsev, S. I., & Zinchenko, R. A.
(2020). Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome. Genes, 11(7), 812.
https://doi.org/10.3390/genes11070812