Found: 3
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Identification of a HOXD13 variant in a Mongolian family with incomplete penetrance syndactyly by exon sequencing.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01360-3
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- Publication type:
- Article
A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family.
- Published in:
- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0781-3
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- Publication type:
- Article
Bidirectional causal link between inflammatory bowel disease and celiac disease: A two-sample mendelian randomization analysis.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.993492
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- Publication type:
- Article