Preimplantation Genetic Diagnosis (PGD) for Monogenic Disorders: the Value of Concurrent Aneuploidy Screening
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://link.springer.com/content/pdf/10.1007/s10897-016-9975-4.pdf
Reference40 articles.
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4. Burlet, P., Frydman, N., Gigarel, N., Kerbrat, V., Tachdjian, G., Feyereisen, E., et al. (2006). Multiple displacement amplification improves PGD for fragile X syndrome. Molecular Human Reproduction, 12(10), 647–652. doi: 10.1093/molehr/gal069 .
5. Campbell, A., Fishel, S., Bowman, N., Duffy, S., Sedler, M., & Hickman, C. F. (2013). Modelling a risk classification of aneuploidy in human embryos using non-invasive morphokinetics. Reproductive Biomedicine Online, 26(5), 477–485. doi: 10.1016/j.rbmo.2013.02.006 .
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