Author:
Mann Kathy,Petek Erwin,Pertl Barbara
Reference26 articles.
1. Lewin P, Kleinfinger P, Bazin A et al (2000) Defining the efficiency of fluorescence in situ hybridization on uncultured amniocytes on a retrospective cohort of 27407 prenatal diagnoses. Prenat Diagn 20(1):1–6
2. Waters JJ, Waters KS (1999) Trends in cytogenetic prenatal diagnosis in the UK: results from UKNEQAS external audit, 1987–1998. Prenat Diagn 19(11):1023–1026
3. Klinger K, Landes G, Shook D et al (1992) Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH). Am J Hum Genet 51(1):55–65
4. Spathas DH, Divane A, Maniatis GM et al (1994) Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective study. Prenat Diagn 14(11):1049–1054
5. Cirigliano V, Voglino G, Ordonez E et al (2009) Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR, results of 9 years of clinical experience. Prenat Diagn 29(1):40–49.
https://doi.org/10.1002/pd.2192
Cited by
2 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