A strategy using SNP linkage analysis for monogenic diseases PGD combined with HLA typing.

This study offers a highly flexible and precise method which could eliminate misdiagnosis caused by chromosomal recombination of the HLA gene, thus potentially benefit the success rate of HSCT. This article is protected by copyright. All rights reserved.
PMID: 32378203 [PubMed - as supplied by publisher]

Source: Clinical Genetics - May 6, 2020 Category: Genetics & Stem Cells Authors: Wang Y, Qin M, Yan Z, Guan S, Kuo Y, Kong S, Nie Y, Zhu X, Zhi X, Qiao J, Yan L Tags: Clin Genet Source Type: research