Non-invasive Prenatal Diagnosis for BRCA Mutations – a Qualitative Pilot Study of Health Professionals’ Views
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://link.springer.com/content/pdf/10.1007/s10897-015-9858-0.pdf
Reference34 articles.
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3. 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, 890–901.
4. Borry, P., Fryns, J. P., Schotsmans, P., & Dierickx, K. (2006a). Carrier testing in minors: a systematic review of guidelines and position papers. European Journal of Human Genetics, 14, 133–138.
5. Borry, P., Stultiens, L., Nys, H., Cassiman, J. J., & Dierickx, K. (2006b). Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers. Clinical Genetics, 70, 374–381.
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