Author:
Kotagal Suresh,Bicknese Alma R.,Eswara Marthand,Fenton Glen A.,Geller Thomas J.,Grange Dorothy K.,Martin David S.,Nigro Michael A.,Pittman Thomas
Reference171 articles.
1. Burnelli S, Faiella A, Capra V, et al.: Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly. Nat Genet 1996, 12:94–96.
2. Dobyns W, Reiner O, Carrozzo R, Ledbetter D: Lissencephaly: a human brain malformation associated with deletion of the LIS-1 gene located on chromosome 17p13. JAMA 1993, 270: 2838–2842.
3. Guttman RH, Collins FS: Recent progress toward understanding the molecular biology of von Recklinghausen’s neurofibromatosis. Ann Neural 1992, 31: 555–561.
4. Use of folic acid for prevention of spina bifida and other neural tube defects-1983–1991. MMWR 1991, 40 (30): 513–516.
5. Recommendations for the use of folic acid to reduce the number of cases of spina bifida and other neural tube defects. MMWR 1992, 41 (RR-14): 1–7.