Publisher
Springer International Publishing
Reference26 articles.
1. Blattner A, Huber AR, Röthlisberger B (2010) Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance. Am J Med Genet A 152a(8):2053–2056
2. Boles RG, Pober BR, Gibson LH, Willis CR, McGrath J, Roberts DJ et al (1995) Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review. Am J Med Genet 55(2):155–160
3. Clark EB (1996) Pathogenetic mechanisms of congenital cardiovascular malformations revisited. Semin Perinatol 20(6):465–472
4. Crackower MA, Scherer SW, Rommens JM, Hui CC, Poorkaj P, Soder S et al (1996) Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development. Hum Mol Genet 5(5):571–579
5. Dai L, Li YH, Deng Y, Zhu J, Wang YP, Liang J et al (2010) Prevalence of congenital split hand/split foot malformation in Chinese population. Sichuan Da Xue Xue Bao Yi Xue Ban 41(2):320–323