Author:
Tint G. S.,Batta Ashok K.,Xu Guorong,Shefer Sarah,Honda Akira,Irons Mira,Elias Ellen Roy,Salen Gerald
Reference137 articles.
1. Abuelo, D., Tint, G. S., Kelley, R., Batta, A. K., Shefer, S., and Salen, G., 1995, Prenatal diagnosis of the cholesterol biosynthetic defect in Smith-Lemli-Opitz syndrome by the analysis of amniotic fluid, Am. J. Med. Genet. 56:281–285.
2. Alley, T. L., Gray, B. A., Lee, S.-H., Scherer, S., Tsui, L.-C., Tint, G. S., Williams, C. A., Zori, R., and Wallace, M. R., 1995, Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient, Am. J. Hum. Genet. 56:1411–1416.
3. Ansari, G. A. S., Walker, R. D., Smart, V. B., and Smith, L. L., 1982, Further investigations of mutagenic cholesterol preparations, Chem. Toxic. 20:35–41.
4. Axelson, M., 1991, Occurrence of isomeric dehydrocholesterols in human plasma, J. Lipid Res. 32:1441–1448.
5. Barbu, V., Roux, C., Lambert, D., Dupuis, R., Gardette, J., and Maziere, J.-C., 1988, Cholesterol prevents the teratogenic action of AY9944: importance of the timing of cholesterol supplementation to rats, J. Nutr. 118:774–779.
Cited by
15 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献