REFERENCES
- Boyles A. L., Billups A. V., Deak K. L., Siegel D. G., Mehltretter L., Slifer S. H., Bassuk A. G., Kessler J. A., Reed M. C., Nijhout H. F., George T. M., Enterline D. S., Gilbert J. R., Speer M. C. Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions. Environmental Health Perspectives 2006; 114: 1547–1552
- Chen C. P., Chern S. R., Lee C. C., Chen W. L., Wang W. Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly. Prenatal Diagnosis 2001; 21: 102–195
- Detrait E. R., George T. M., Etchevers H. C., Gilbert J. R., Vekemans M., Speer M. C. Human neural tube defects: Developmental biology, epidemiology, and genetics. Neurotoxicology and Teratology 2005; 27: 515–524
- Elena S. F., Cooper V. S., Lenski R. E. Punctuated evolution caused by selection of rare beneficial mutations. Science 1996; 272: 1802–1804
- Hahm G. K., Barth R., Schauer G. M., Reiss R., Opitz J. M. Trisomy 2p syndrome: A fetus with anencephaly and postaxial polydactyly. American Journal of Medical Genetics 1999; 87: 45–48
- Hrdlicka A. Children running on all fours. American Journal of Physical Anthropology 1928; 11: 149–185
- Koukoura O., Sifakis S., Stratoudakis G., Mantas N., Kaminopetros P., Koumantis E. A case report of recurrent on encephaly and literature review. Clinical and Experimental Obstetrics & Gynecology 2006; 33: 185–189
- Lemire R. J. Neural tube defects. JAMA 1988; 259: 558–562
- Lomholt J. F., Fisher-Hanen B., Keeling J. W., Reintoft I., Kjaer I. Subclassification of anencephalic human fetuses according to morphology of the posterior cranial fossa. Pediatric and Developmental Pathology 2004; 7: 601–606
- Lynch S. A. Non-multifactorial neural tube defects. American Journal of Medical Genetics, Part C 2005; 135C: 69–76
- Mezhzherin S. V. Gradualism or puntualism: Data on genetic differentiation of small mammals from the Holarctic region. Genetika 1997; 33: 518–523
- Minghetti P. P., Dugaiczyk A. The emergence of new DNA repeats and the divergence of primates. Proceedings of National Academy of Sciences, U S A 1993; 90: 1872–1876
- Mitchell L. E. Epidemiology of neural tube defects. American Journal of Medical Genetics 2005; 135C: 88–94
- Polanski J. M., Franciscus R. G. Patterns of craniofacial integration in extant homo, pan, and gorilla. American Journal of Physical Anthropology 2006; 131: 38–49
- Porter M. L., Crandall K. A. Lost along the way: The significance of evolution in reverse. Trends in Ecology and Evolution 2003; 18: 541–547
- Rushton J. P., Ankney C. D. Size matters: A review and new analysis of racial differences in cranial capacity and intelligence that refute Kamin and Omari. Personality and Individual Differences 2000; 29: 591–620
- Tan Ü. Unertan Syndrome; qaudrupedality, primitive language, and severe mental retardation; a new theory on the evolution of human mind. NeuroQuantology 2005; 4: 250–255
- Tan Ü. A new syndrome with quadrupedal gait, primitive speech, and severe mental retardation as a live model for human evolution. International Journal of Neuroscience 2006a; 116: 361–369
- Tan Ü. Evidence for “Unertan Syndrome” and the evolution of the human mind. International Journal of Neuroscience 2006b; 116: 763–774
- Tan Ü. Evidence for “Uner Tan Syndrome” as a human model for reverse evolution. International Journal of Neuroscience 2006c; 116: 1433–1441
- Tasdelen E., Arvas A., Perk Y., Ilter O. An evaluation of the cases of neural tube defects. Cerrapasa Journal of Medicine 1996; 27: 59–62
- Tvrdik P., Capecchi M. R. Reversal of Hox1 gene subfunctionalization in the mouse. Developmental Cell 2006; 11: 239–250
- Wahlsten D. Single-gene influence on brain and behavior. Annual Review of Psychology 1999; 50: 599–624