Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses

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.

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