“Classical cytogenetics” is not equal to “banding cytogenetics”
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry
Link
http://link.springer.com/content/pdf/10.1186/s13039-017-0305-9.pdf
Reference17 articles.
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2. Srebniak MI, Boter M, Oudesluijs GO, Cohen-Overbeek T, Govaerts LC, Diderich KE, et al. Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities. Mol Cytogenet. 2012;5:14.
3. Kooper AJ, Pieters JJ, Faas BH, Hoefsloot LH, van der Burgt I, Zondervan HA, et al. Is routine karyotyping required in prenatal samples with a molecular or metabolic referral? Mol Cytogenet. 2012;5:7.
4. Park SJ, Jung EH, Ryu RS, Kang HW, Ko JM, Kim HJ, et al. Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases. Mol Cytogenet. 2011;4:12.
5. Fauzdar A. Non-invasive prenatal testing (NIPT): a better option for patients. Mol Cytogenet. 2014;7:I17.
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