References
- Benacerraf B R, Frigoletto F D, Laboda L A, et al. Sonographic diagnosis of Down syndrome in the second trimester. American Journal of Obstetrics and Gynecology 1985; 153: 49–52
- De Ravel T J, Thiry P, Fryns J P, et al. Follow up of adult males with chromosome 18p deletion. European Journal of Medical Genetics 2005; 34: 189–193
- Robson M, Pearce M. Neck and thorax malformations. Prenatal diagnosis in obstetric practice, M J Whittle, J M Connor. Blackwell Science, London 1995
- Schinzel A, Schmid W, Luscher U, et al. Structural aberrations of chromosome 18. The 18p-syndrome. Archiv für Genetik (Zurich) 1974; 47: 1–15
- Tsukahara M, Imaizumi K, Fujita K, et al. Familial Del(18p) syndrome. American Journal of Medical Genetics 2001; 99: 67–69
- Turleau C. Monosomy 18p. Orphanet Journal of Rare Diseases 2008; 3: 4
- Vasquez J C, Rabah R, Delius R E, et al. Hypoplastic left heart syndrome with intact atrial septum associated with deletion of the short arm of chromosome 18. Cardiovascular Pathology 2003; 12: 102–104
- Wong H S, Lam Y H, Tang M H, et al. First-trimester ultrasound diagnosis of holoprosencephaly: three case reports. Ultrasound in Obstetrics and Gynecology 1999; 13: 356–359
- Young-Mi K, Eun-Hee C, Jin-Mi K, et al. Del(18p) syndrome with increased nuchal translucency in prenatal diagnosis. Prenatal Diagnosis 2004; 3: 161–164