Funder
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference50 articles.
1. D’Amours G, Langlois M, Mathonnet G, Fetni R, Nizard S, Srour M, et al. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay. BMC Med Genet. 2014;7:70.
2. Delgado F, Tabor HK, Chow PM, Conta JH, Feldman KW, Tsuchiya KD, et al. Single nucleotide polymorphism (SNP) arrays and unexpected consanguinity: considerations for clinicians when returning results to families HHS public access. Genet Med. 2015;17:400–4.
3. Choucair N, Ghoch JA, Corbani S, Cacciagli P, Mignon-Ravix C, Salem N, et al. Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients. Mol Cytogenet. 2015;8:26.
4. Papenhausen P, Schwartz S, Risheg H, Keitges E, Gadi I, Burnside RD, et al. UPD detection using homozygosity profiling with a SNP genotyping microarray. Am J Med Genet Part A. 2011;155:757–68.
5. Wiszniewska J, Bi W, Shaw C, Stankiewicz P, Kang S-HL, Pursley AN, et al. Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing. Eur J Hum Genet. 2014;22:79–87.
Cited by
16 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