References
- Cho RC, Chu P, Smith-Bindman R. 2009. Second trimester prenatal ultrasound for the detection of pregnancies at increased risk of Trisomy 18 based on serum screening. Prenatal Diagnosis 29:129–139.
- Kariminejad A, Kariminejad R, Moshtagh A . 2011. Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18. European Journal of Human Genetics 19:555–560.
- Martin AO, Simpson JL, Deddish RB . 1983. Clinical implications of chromosomal inversions. A pericentric inversion in No. 18 segregating in a family ascertained through an abnormal proband. American Journal of Perinatology 1:81–88.
- Ogilvie CM, Donaghue C, Fox SP . 2005. Rapid prenatal diagnosis of aneuploidy using quantitative fluorescence-PCR (QF-PCR). Journal of Histochemistry and Cytochemistry 53:285–288.
- Prabhakara K, Wyandt HE, Huang XL . 2004. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18. Annales de Genetique 47:297–303.
- Vermeulen SJ, Speleman F, Vanransbeeck L . 2005. Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome. European Journal of Human Genetics 3:52–58.
- Vianna-Morgante AM, Nozaki MJ, Ortega CC . 1976. Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18. Journal of Medical Genetics 13:366–370.