Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome

OBJECTIVES: To evaluate the performance of a single‐nucleotide polymorphism (SNP)‐based non‐invasive prenatal test (NIPT) for the detection of fetal 22q11.2 deletion syndrome in clinical practice, assess clinical follow‐up and review patient choices for women with high‐risk results. METHODS: In this...

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Detalles Bibliográficos
Autores principales: Gross, S. J., Stosic, M., McDonald‐McGinn, D. M., Bassett, A. S., Norvez, A., Dhamankar, R., Kobara, K., Kirkizlar, E., Zimmermann, B., Wayham, N., Babiarz, J. E., Ryan, A., Jinnett, K. N., Demko, Z., Benn, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2016
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064640/
https://www.ncbi.nlm.nih.gov/pubmed/26396068
http://dx.doi.org/10.1002/uog.15754

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064640/
https://www.ncbi.nlm.nih.gov/pubmed/26396068
http://dx.doi.org/10.1002/uog.15754

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