Ann Lab Med 2017; 37(6): 563-565  
Phenotype of a Patient With a 1p36.11-p35.3 Interstitial Deletion Encompassing the AHDC1
Hae-Yeon Park, M.D.1, Myungshin Kim, M.D.2,3, Woori Jang, M.D.2,3, and Dae-Hyun Jang, M.D.1
Department of Rehabilitation Medicine1, College of Medicine, The Catholic University of Korea, Incheon St. Mary’s Hospital, Incheon; Department of Laboratory Medicine2, College of Medicine, The Catholic University of Korea, Seoul; Catholic Genetic Laboratory Center3, College of Medicine, The Catholic University of Korea, Seoul, Korea
Correspondence to: Dae-Hyun Jang
Department of Rehabilitation medicine, Incheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 56 Dongsu-ro, Bupyeong-gu, Incheon 21431, Korea
Tel: +82-32-280-5207, Fax: +82-32-280-5040 E-mail: dhjangmd@naver.com
Received: January 6, 2017; Revised: March 8, 2017; Accepted: July 6, 2017; Published online: November 1, 2017.
© The Korean Society for Laboratory Medicine. All rights reserved.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


This Article

e-submission

Archives

Indexed/Covered by