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1 Chromosomal Deletion in 7q31.2-31.32 Involving Ca2+-Dependent Activator Protein for Secretion Gene in a Patient with Cerebellar Ataxia: a Case Report
Seungbeen Hong, Su Ji Lee, Sung-Rae Cho
Brain Neurorehabil.2020;13(1):e9.  Published online 2019 December 16     DOI: http://dx.doi.org/10.12786/bn.2020.13.e9
      
2 Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3
Asayeon Choi, Ja-Young Oh, Myungshin Kim, Woori Jang, Dae-Hyun Jang
Ann Rehabil Med.2017;41(5):881-886.   Published online 2017 October 31     DOI: http://dx.doi.org/10.5535/arm.2017.41.5.881
   
3 Identification of a Novel Deletion Region in 3q29 Microdeletion Syndrome by Oligonucleotide Array Comparative Genomic Hybridization
Eul-Ju Seo, Kyung Ran Jun, Han-Wook Yoo, Hanik K. Yoo, Jin-Ok Lee
Korean J Lab Med.2010;30(1):70-75.   Published online 2010 January 14     DOI: http://dx.doi.org/10.3343/kjlm.2010.30.1.70
   

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