Publication catalog

Biomedical publications with connected research

Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.

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Publications

Page 7535 of 10600

  1. A novel gene mutation of Runx2 in cleidocranial dysplasia.

    Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban | 2017-10-01 | PMID 29058294

    Peng You-Jian, Chen Qiao-Yun, Fu Dong-Jie and 4 more

    Genes: RUNX2, CAT, TAT