Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://link.springer.com/content/pdf/10.1007/s10897-012-9564-0
Reference16 articles.
1. Ashoor, G., Syngelaki, A., Wang, E., Struble, C., Oliphant, A., Song, K., et al. (2012). Trisomy 13 detection in the first trimester of pregnancy using a chromosome-selective cell-free DNA analysis method. Ultrasound in Obstetrics & Gynecology. doi: 10.1002/uog.12299 [Epub ahead of print].
2. Benn, P., Borrell, A., Cuckle, H., Dugoff, L., Gross, S., Johnson, J. A., et al. (2012a). Prenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011. Prenatal Diagnosis, 32(1), 1–2. doi: 10.1002/pd.2919 .
3. Benn, P., Cuckle, H., & Pergament, E. (2012b). Non-invasive prenatal diagnosis for Down syndrome: the paradigm will shift, but slowly. Ultrasound in Obstetrics & Gynecology, 39(2), 127–130. doi: 10.1002/uog.11083 .
4. Bianchi, D. W., Platt, L. D., Goldberg, J. D., Abuhamad, A. Z., Sehnert, A. J., & Rava, R. P. (2012). Genome-Wide Fetal Aneuploidy Detection by Maternal Plasma DNA Sequencing. Obstetrics and Gynecology, 119(5), 1–13.
5. Chan, K., Yam, I., Leung, K. Y., Tang, M., Chan, T. K., & Chan, V. (2010). Detection of paternal alleles in maternal plasma for non-invasive prenatal diagnosis of beta-thalassemia: a feasibility study in southern Chinese. European Journal of Obstetrics, Gynecology, and Reproductive Biology, 150(1), 28–33.
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