Author:
Forabosco Antonino,Percesepe Antonio,Santucci Sandra
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference26 articles.
1. Hook EB, Hamerton JL : The frequency of chromosome abnormalities detected in consecutive newborn studies; difference between studies; results by sex and severity of phenotypic involvement; in Hook EB, Porter IH (eds): Population Cytogenetics: Studies in Humans. New York: Academic Press, 1977, pp 63–79.
2. Benn PA, Hsu LYF : Prenatal diagnosis of chromosomal abnormalities through amniocentesis; in Milunsky A (ed): Genetic Disorders and the Fetus, 5th edn. Baltimore: The Johns Hopkins University Press, 2004, pp 214–296.
3. Ferguson-Smith MA, Yates JR : Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses. Prenat Diagn 1984; 4 (Spec No): 5–44.
4. Hook EB, Cross PK, Schreinemachers DM : Chromosomal abnormality rates at amniocentesis and in live-born infants. JAMA 1983; 249: 2034–2038.
5. Wapner R, Thom E, Simpson JL et al: First-trimester screening for trisomies 21 and 18. N Engl J Med 2003; 349: 1405–1413.
Cited by
87 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