References
- 1. Drăgusin RC, Sorop-Florea M, Pătru CL, et al. Fetal abdominal wall defects. In: Tudorache S. Congenital anomalies: From the embryo to the neonate. IntechOpen 2018:207-230.10.5772/intechopen.71936
- 2. Peterson JF, Ghaloul-Gonzalez L, Madan-Khetarpal S, et al. Familial microduplication of 17q23.1–q23.2 involving TBX4 is associated with congenital clubfoot and reduced penetrance in females. Am J Med Genet A 2014;164A(2):364-910.1002/ajmg.a.36238
- 3. Alvarado DM, Aferol H, McCall K, et al. Familial isolated clubfoot is associated with recurrent chromosome 17q23.1q23.2 microduplications containing TBX4. Am J Hum Genet 2010;87(1):154-160.10.1016/j.ajhg.2010.06.010
- 4. Pakdaman R, Woodward PJ, Kennedy A. Complex abdominal wall defects: Appearances at prenatal imaging. Radiographics 2015;35(2):636-649.10.1148/rg.352140104
- 5. Wilson RD, Johnson MP. Congenital abdominal wall defects: an update. Fetal Diagn Ther 2004; 19(5):385-98.10.1159/000078990
- 6. Van Allen MI, Curry C, Walden C, et al. Limb body wall complex: II. Limb and spine defects. Am J Med Genetics 1987;28(3):549-65.10.1002/ajmg.1320280303
- 7. Chen CP. Chromosomal abnormalities associated with omphalocele. Taiwan J Obstet Gynecol 2007;46(1):1-8.10.1016/S1028-4559(08)60099-6