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Journal: Genes, 2020
Volume: 11
Number: 812
Article:
Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome
Authors:
by
Tatyana A. Vasilyeva, Andrey V. Marakhonov, Natella V. Sukhanova, Sergey I. Kutsev and Rena A. Zinchenko
Link:
https://www.mdpi.com/2073-4425/11/7/812
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