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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://0-www-mdpi-com.brum.beds.ac.uk/2073-4425/11/7/812

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