A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe Obesity

Lu, H. C., Fang, W., Chen, W. L., Chaou, W. T., Wang, Y. M., & Wang, B. T. (2001). Molecular Studies on Small Ring X Chromosome in a Female with a Severe Phenotype. Journal of Genetics and Molecular Biology, 12(2), 85-92. https://doi.org/10.30047/JGMB.200106.0004
Hu, J., Khetarpal, S. M., Russi, A. H. S., Kochmar, S., DeWard, S. J., Sathanoori, M., & Surti, U. (2011). Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features. Genetics Research International, 2011(), 5-11. https://doi.org/10.4061/2011/185271
Fan, H. C., Yue, C. T., Chi, C. S., Liou, S. Y., Lin, C. Y., & Cheng, S. N. (2021). Maternal Inheritance of Deletion of Chromosome 18 q21.3. 童綜合醫學雜誌, 15(S), 62-66. https://doi.org/10.3966/20713592202109150S009
Chen, C. P., Chern, S. R., Wu, P. C., Tsai, F. J., Lee, C. C., Town, D. D., Chen, W. L., Chen, L. F., Lee, M. S., Pan, C. W., & Wang, W. (2009). Unbalanced and Balanced Acrocentric Rearrangements Involving Chromosomes Other Than Chromosome 21 at Amniocentesis. Taiwanese Journal of Obstetrics & Gynecology, 48(4), 389-399. https://doi.org/10.29787/TJOG.200912.0010
Wu, K. H., Yu, M. T., Tsai, F. J., Peng, C. T., & Tsai, C. H. (2002). Monosomy of Chromosome 10q26 with Mild Psychomotor Retardation: Report of One Case. Acta Paediatrica Taiwanica, 43(3), 153-156. https://doi.org/10.7097/APT.200206.0153