REFERENCES
- Pilu G, Nicolaides K. Diagnosis of fetal abnormalities. Parthenon Publishing Group. 1999, The 18–23 weeks scan
- Pilu G, Sandri F, Perolo A. Sonography of fetal agenesis of the corpus callosum: a survey of 35 cases. Ultrasound Obstet Gynecol 1993; 3: 318–329
- Romero R, Pilu G, Jeanty P. Prenatal Diagnosis of Congenital Anomalies. Appleton and Lange, Norwalk, CT, San Mateo, CA 1988
- Kendall E. Dysgenesis of the corpus callosum. Neuroradiology 1983; 25: 239
- Rakic P, Yakovlev P I. Development of the corpus callosum and cavum septi in man. J Comp Neurol 1968; 132: 45
- Probst F P. Congenital defects of the corpus callosum: morphology and encephalographic appearances. Acta Radiol (Diag) 1973; 331: 1S
- Harris R J, Haas L. Septo-optic dysplasia with growth hormone deficiency (de Morsier syndrome). Arch Dis Child 1972; 47: 973–976
- Morishima A, Aranoff G S. Syndrome of septo-optic-pituitary dysplasia: the clinical spectrum. Brain Dev 1986; 8: 233–239
- Barkovich A J, Norman D. Absence of the septum pellucidum: a useful sign in the diagnosis of congenital brain malformations. Am J Roentgenol 1989; 152: 353–360
- Nyberg D A, Mack L A, Bronstein A, Hirsh J, Pagon R A. Holoprosencephaly: prenatal sonographic diagnosis. Am J Roentgenol 1987; 149: 1051–1058
- Birnholz J C. Septum pellucidum fenestration: visualization by ultrasound. Am J Roentgenol 1983; 149: 122
- Aicardi J. Malformations of the central nervous system. Diseases of the Nervous System in Childhood, J Aicardi. MacKeith Press UK, London 1998; 87–89
- Malinger G, Lev D, Kidron D, Heredia F, Hershkovitz R, Lerman-Sagie T. Differential diagnosi in fetuses with absent septum pellucidim. Ultrasound Obstet Gynecol 2005; 25: 42–49
- Gupta J K, Lilford R J. Assessment and management of fetal agenesis of the corpus callosum. Prena Diag 1995; 15: 301–312
- Vergani P, Ghidini A. Strobelt N Prognostic indicators in the prenatal diagnosis of agenesis of the corpus callosum. Am J Obstet Gynecol 1994; 170: 753–758
- Robert E. Teratogen update: electromagnetic fields. Teratology 1995; 54: 305–313
- Robert E. Intrauterine effects of electromagnetic fields–(low frequency, mid-frequency RF, and microwave): review of epidemiologic studies. Teratology 1999; 59: 292–298
- Repacholi M H. Low-level exposure to radiofrequency electromagnetic fields: health effects and research needs. Bioelecytromagnetics 1998; 19: 1–19
- Ketchen E E, Porter W E, Bolton N E. The biological effects of magnetic fields on man. Am Ind Hyg Assoc J 1978; 39: 1–11
- Nordenson I, Mild K H, Andersson G, Sandstrom M. Chromosomal aberrations in human amniotic cells after intermittent exposure to fifty hertz magnetic fields. Bioelectromagnetics 1994; 15: 293–301
- Winker R, Ivancsits S, Pilger A, Adlkofer F, Rüdiger H W. Chromosomal damage in human diploid fibroblasts by intermittent exposure to extremely low-frequency electromagnetic fields. Mutat Res 2005; 585: 43–39
- Wolf F I, Torsello A, Tedesco B, Fasanella S, Boninsegna A, D'Ascenzo M, Grassi C, Azzena G B, Cittadini A. 50-Hz extremely low frequency electromagnetic fields enhance cell proliferation and DNA damage: possible involvement of a redox mechanism. Biochim Biophys Acta 2005; 1743: 120–129