Author:
KATAOKA AKIO,HIRAKAWA SHOUKO,IWAMOTO MANAMI,SAKUMURA YUMI,YOSHINAGA RYOUTA,OHBA TAKASHI
Reference18 articles.
1. 1. Allderdice PW, Davis JG, Miller OJ, Warburton D, Miller DA et al. The 13q- deletion syndrome. Am J Hum Genet 1969; 21:499-512.
2. 3. Sanker VH, and Phadke S. Ring chromosome 13 in an infant with ambiguous ganitalia. Indian Pediatrics 2006; 43:258-260.
3. 4. Guitierrez J, Sepulveda W, Saez R, Carstens E, and Sanchez J. Prenatal diagnosis of 13q- syndrome in a fetus with holoprosencephaly and thum agenesis. Ultrasounf Obstete Gynecol 2001; 17:166-168.
4. 5. Chen CP, Liu FF, Jan SW, Wang KG, and Lan CC. Prenatal diagnosis of partial monosomy 13q associated with occipital encephalocoele in fetus. Prenat Diagn 1996; 16:664-666.
5. 6. Edward AJ, Helio AGF, Claudio RP, and Sebastiao MZF. Prenatal diagnosis of the 13q- syndrome through three-dimensional ultrasonography: a case report. Archives of Gynecol and Obstet 2006; 274:243-245.
Cited by
4 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