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Journal Abstract Search

149 related items for PubMed ID: 18072967

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  • 3. [HOXD13 polyalanine tract expansion in synpolydactyly: mutation detection and prenatal diagnosis in a large Chinese family].
    Zhao XL, Meng JP, Sun M, Ao Y, Wu AH, Lo HY, Zhang X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):5-9. PubMed ID: 15696469
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  • 9. A Novel Missense Variant of HOXD13 Caused Atypical Synpolydactyly by Impairing the Downstream Gene Expression and Literature Review for Genotype-Phenotype Correlations.
    Guo R, Fang X, Mao H, Sun B, Zhou J, An Y, Wang B.
    Front Genet; 2021 Feb; 12():731278. PubMed ID: 34777468
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  • 10. 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.
    Am J Hum Genet; 1998 Oct; 63(4):992-1000. PubMed ID: 9758628
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  • 12. Eight-alanine duplication in homeobox D13 in a Chinese family with synpolydactyly.
    Xin Q, Li L, Li J, Qiu R, Guo C, Gong Y, Liu Q.
    Gene; 2012 May 10; 499(1):48-51. PubMed ID: 22406499
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  • 16. [Genetic analysis of a Chinese pedigree with congenital synpolydactyly].
    Qin W, Shu AL, Xing QH, Yang MS, Feng GY, He L.
    Yi Chuan Xue Bao; 2003 Oct 10; 30(10):973-7. PubMed ID: 14669516
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  • 18. Mutation analysis of HOXD13 gene in a Chinese pedigree with synpolydactyly.
    Dai L, Heng ZC, Zhu J, Cai R, Mao M, Wang H, Lin MJ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun 10; 22(3):277-80. PubMed ID: 15952114
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  • 19. A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactyly.
    Jia W, Zhou X, Guo N, Zhang D, Hou M, Luo Y, Peng X, Yang X, Zhang X.
    Am J Med Genet A; 2022 Jan 10; 188(1):31-36. PubMed ID: 34467619
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  • 20. Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families.
    Akarsu AN, Stoilov I, Yilmaz E, Sayli BS, Sarfarazi M.
    Hum Mol Genet; 1996 Jul 10; 5(7):945-52. PubMed ID: 8817328
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