Chromosome 2q14.3 microdeletion encompassing CNTNAP5 gene in a patient carrying a complex chromosomal rearrangement
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
https://link.springer.com/content/pdf/10.1007/s12041-021-01316-z.pdf
Reference16 articles.
1. Alarcon M., Abrahams B. S., Stone J. L., Duvall J. A., Perederiy J. V., Bomar J. M. et al. 2008 Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am. J. Hum. Genet. 82, 150–159.
2. Allen J. D. and Bishop J. R. 2019 A systematic review of genome-wide association studies of antipsychotic response. Pharmacogenomics 20, 291–306.
3. Ballarati L., Recalcati M. P., Bedeschi M. F., Lalatta F., Valtorta C., Bellini M. et al. 2009 Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient. Eur. J. Med. Genet. 52, 218–223.
4. Berisha S. Z., Serre D., Schauer P., Kashyap S. R. and Smith J. D. 2011. Changes in whole blood gene expression in obese subjects with type 2 diabetes following bariatric surgery: a pilot study. PLoS One. 6, e16729.
5. Chen Q., Huang B., Zhan J., Wang J., Qu K., Zhang F. et al. 2020 Whole-genome analyses identify loci and selective signals associated with body size in cattle. J. Anim. Sci. 98.
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1. Prenatal Diagnosis of a de novo 2q14.3-q22.1 Deletion with Complex Chromosomal Rearrangement;Molecular Syndromology;2023-09-18
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