Importance of embryo aneuploidy screening in preimplantation genetic diagnosis for monogenic diseases using the karyomap gene chip
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-21094-6.pdf
Reference19 articles.
1. Dreesen, J. et al. Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study. Eur J Hum Genet. 22, 1012–1018 (2014).
2. Zamani Esteki, M. et al. Concurrent whole-genome haplotyping and copy-number profiling of single cells. Am J Hum Genet. 96, 894–912 (2015).
3. Dimitriadou, E. et al. Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos. Hum Reprod. 32, 687–697 (2017).
4. Yan, L. et al. Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses. Proc Natl Acad Sci. 112, 15964–15969 (2015).
5. Handyside, A. H. et al. Karyomapping: a universal method for genome wide analysis of genetic disease based on mapping crossovers between parental haplotypes. J Med Genet. 47, 651–658 (2010).
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