Next-Generation Sequencing-Based Preimplantation Genetic Testing for De Novo NF1 Mutations-Reference-Cited by-同舟云学术

Next-Generation Sequencing-Based Preimplantation Genetic Testing for De Novo NF1 Mutations

Published:2021-02-22 Issue:1 Volume:15 Page:69-76
ISSN:1976-0280
Container-title:BioChip Journal
language:en
Short-container-title:BioChip J

Author:

Chen Dongjia,Shen Xiaoting,Xu Yan,Cai Bing,Ding Chenhui,Zhong Yiping,Xu Yanwen,Zhou Canquan^ORCID

Funder

Guangdong Provincial Key Laboratory of Reproductive Medicine

Guangzhou Science and Technology Project: Development and Application of The Reagents for Preimplantation Diagnosis and Screening by Next-Generation Sequencing

Publisher

Springer Science and Business Media LLC

Subject

Electrical and Electronic Engineering,Biomedical Engineering,Bioengineering,Biotechnology

Link

http://link.springer.com/content/pdf/10.1007/s13206-021-00006-3.pdf

Reference45 articles.

1. Evans, D.G., Howard, E., Giblin, C., Clancy, T., Spencer, H., Huson, S.M., Lalloo, F.: Birth incidence and prevalence of tumor-prone syndromes: estimates from a UK family genetic register service. Am. J. Med. Genet. Part A 152a, 327–332 (2010)

2. Gutmann, D.H., Ferner, R.E., Listernick, R.H., Korf, B.R., Wolters, P.L., Johnson, K.J.: Neurofibromatosis type 1. Nat Rev. Dis. Primers 3, 17004 (2017)

3. Rad, E., Tee, A.R.: Neurofibromatosis type 1: fundamental insights into cell signalling and cancer. Semin. Cell Dev. Biol. 52, 39–46 (2016)

4. Uusitalo, E., Rantanen, M., Kallionpää, R.A., Pöyhönen, M., Leppävirta, J., Ylä-Outinen, H., Riccardi, V.M., Pukkala, E., Pitkäniemi, J., Peltonen, S., Peltonen, J.: Distinctive cancer associations in patients with neurofibromatosis type 1. J. Clin. Oncol. 34, 1978–1986 (2016)

5. Evans, D.G., O’hara, C., Wilding, A., Ingham, S.L., Howard, E., Dawson, J., Moran, A., Scott-Kitching, V., Holt, F., Huson, S.M.: Mortality in neurofibromatosis 1: in North West England: an assessment of actuarial survival in a region of the UK since 1989. Eur. J. Hum. Genet. 19, 1187–1191 (2011)

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A point-of-care platform for hair loss-related single nucleotide polymorphism genotyping;Analytica Chimica Acta;2023-12

2. Application of the PGT-M strategy using single sperm and/or affected embryos as probands for linkage analysis in males with hereditary tumor syndromes without family history;Journal of Human Genetics;2023-08-18

3. Zinc-Finger-Protein-Based Microfluidic Electrophoretic Mobility Reversal Assay for Quantitative Double-Stranded DNA Analysis;BioChip Journal;2021-11-10