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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1998 | 1 |
2012 | 1 |
2019 | 1 |
2024 | 0 |
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Isolated brachydactyly type E caused by a HOXD13 nonsense mutation: a case report.
BMC Med Genet. 2012 Jan 10;13:4. doi: 10.1186/1471-2350-13-4.
BMC Med Genet. 2012.
PMID: 22233338
Free PMC article.
A Nonsense Mutation in HOXD13 Gene from A Chinese Family with Non-Syndromic Synpolydactyly.
Guo X, Shi T, Lin M, Zhang Y.
Guo X, et al.
Tohoku J Exp Med. 2019 Oct;249(2):93-100. doi: 10.1620/tjem.249.93.
Tohoku J Exp Med. 2019.
PMID: 31611522
Free article.
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Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families.
Goodman F, Giovannucci-Uzielli ML, Hall C, Reardon W, Winter R, Scambler P.
Goodman F, et al.
Am J Hum Genet. 1998 Oct;63(4):992-1000. doi: 10.1086/302070.
Am J Hum Genet. 1998.
PMID: 9758628
Free PMC article.
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