Clinical Genetic Testing Options
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-52215-5_35
Reference16 articles.
1. Wallace SE, Bean LJ. Educational materials; Genetic Testing: Current Approaches. GeneReviews. 2018. https://www.ncbi.nlm.nih.gov/books/NBK279899/. Accessed 11 November 2019.
2. Dugoff L, Norton ME, Kuller JA. The use of chromosomal microarray for prenatal diagnosis. Am J Obstet Gynecol. 2016;215(4):B2:B9. https://doi.org/10.1016/j.ajog.2016.07.016.
3. Neill NJ, Ballif BC, Lamb AN, Parikh S, Ravnan JB, Schultz RA, et al. Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH. Genome Res. 2011;21(4):535–44. https://doi.org/10.1101/gr.114579.110.
4. Kang SHL, Shaw C, Ou Z, Eng PA, Cooper ML, Pursley AN, et al. Insertional translocation detected using FISH confirmation of array-comparative genomic hybridization (aCGH) results. Am J Med Genet. 2010;152A(5):1111–26. https://doi.org/10.1002/ajmg.a.33278.
5. Kearney HM, South ST, Wolff DJ, Lamb A, Hamosh A, Rao KW. American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities. Genet Med. 2011;13(7):676–9. https://doi.org/10.1097/GIM.0b013e31822272ac.
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