Jianbo Shao to Polymorphism, Single Nucleotide
This is a "connection" page, showing publications Jianbo Shao has written about Polymorphism, Single Nucleotide.
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Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review. BMC Med Genet. 2017 12 01; 18(1):141.
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