![](/img/cover-not-exists.png)
Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome
Vasilyeva, Tatyana A., Marakhonov, Andrey V., Sukhanova, Natella V., Kutsev, Sergey I., Zinchenko, Rena A.Volume:
11
Journal:
Genes
DOI:
10.3390/genes11070812
Date:
July, 2020
File:
PDF, 453 KB
2020