1. Nguyen, Trang Thi Thu, Park, Wei Sun, Park, Byung Ouk, Meyer, Tobias, Heo, Won Do. 2016. PLEKHG3 enhances polarized cell migration by activating actin filaments at the cell front. In Proceedings of the National Academy of Sciences of the United States of America, 113, 10091-6. doi:10.1073/pnas.1604720113. https://pubmed.ncbi.nlm.nih.gov/27555588/
2. Zhu, Yimin, Wu, Xiuhua, Zhang, Yunjiao, Zhou, Rongwei, Guo, Zhong. 2024. Single cell transcriptomic analysis reveals tumor immune infiltration by NK cells gene signature in lung adenocarcinoma. In Heliyon, 10, e33928. doi:10.1016/j.heliyon.2024.e33928. https://pubmed.ncbi.nlm.nih.gov/39071697/
3. Hadži, San, Kocman, Vojč, Oblak, Domen, Plavec, Janez, Lah, Jurij. 2019. Energetic Basis of AGCGA-Rich DNA Folding into a Tetrahelical Structure. In Angewandte Chemie (International ed. in English), 58, 2387-2391. doi:10.1002/anie.201813502. https://pubmed.ncbi.nlm.nih.gov/30620431/
4. Griswold, Anthony J, Ma, Deqiong, Sacharow, Stephanie J, Gilbert, John R, Pericak-Vance, Margaret A. 2011. A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis. In Autism research : official journal of the International Society for Autism Research, 4, 221-7. doi:10.1002/aur.186. https://pubmed.ncbi.nlm.nih.gov/21360829/
5. Maden Bedel, Fayize, Balasar, Özgür, Şimşek, Ayşe, Tokgöz, Hüseyin, Çaksen, Hüseyin. 2024. Could the 14q23.2 microdeletion or AKAP5 haploinsufficiency be a potential cause of intellectual disability? In Psychiatric genetics, 34, 71-73. doi:10.1097/YPG.0000000000000368. https://pubmed.ncbi.nlm.nih.gov/38690958/
6. Lehalle, Daphné, Sanlaville, Damien, Guimier, Anne, Lyonnet, Stanislas, Amiel, Jeanne. 2014. Multiple congenital anomalies-intellectual disability (MCA-ID) and neuroblastoma in a patient harboring a de novo 14q23.1q23.3 deletion. In American journal of medical genetics. Part A, 164A, 1310-7. doi:10.1002/ajmg.a.36452. https://pubmed.ncbi.nlm.nih.gov/24665034/
7. Lybaek, H, Øyen, N, Fauske, L, Houge, G. 2008. A 2.1 Mb deletion adjacent but distal to a 14q21q23 paracentric inversion in a family with spherocytosis and severe learning difficulties. In Clinical genetics, 74, 553-9. doi:10.1111/j.1399-0004.2008.01072.x. https://pubmed.ncbi.nlm.nih.gov/18717686/