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Compound heterozygous missense and intronic variants in B9D1 contribute to a recurrent Meckel syndrome pedigree by Huining Jing, Huining Jing, Bocheng Xu, Bocheng Xu, Hao Wang, Hao Wang, Shanling Liu, Shanling Liu, He Wang, He Wang, Jingqun Mai, Jingqun Mai, Wencong Yao, Wencong Yao, Zhu Zhang, Zhu Zhang
Published 2025-08-01Get full text
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