• Low-frequency Mosaicism of Trisomy 14, Missed by Array CGH

• Lee Cha-Gon

• Yun Jun-No, Park Sang-Jin, Sohn Young-Bae

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.1 52 ~ 56

• Neurovascular Manifestation of Loeys-Dietz Syndrome: A Case Report

• Lee Yun-Jeong

• Yum Mi-Sun, Kim Eun-Hee, Choi Hae-Won, Lee Beom-Hee, Yoo Han-Wook, Ko Tae-Sung

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.1 47 ~ 51

• An Incidentally Identified Sporadic Case with Adrenoleukodystrophy with the ABCD1 Mutation

• Shin Soon-Jung

• Kim Ja-Hye, Kim Yoo-Mi, Kim Gu-Hwan, Lee Beom-Hee, Yoo Han-Wook

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.1 43 ~ 46

• Clinical Experiences of Molecular Genetic Evaluation of Achondroplasia in Prenatal and Neonatal Case...

• Kwak Dong-Wook

• Kim Hyun-Jin, Park So-Yeon, Ahn Hyun-Suk, Chae Yong-Hwa, Kim Moon-Young, Lee Young-Ha, Ryu...

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.1 38 ~ 42

• Southern Analysis after Long-range PCR: Clinical Application in Korean Patients with Myotonic Dystro...

• Yum Mi-Sun

• Lee Beom-Hee, Kim Gu-Hwan, Lee Jin-Joo, Choi Seung-Hoon, Lee Joo-Yeon, Kim Jae-Min, Kim Yo...

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.1 33 ~ 37

• Bioinformatics Approaches for the Identification and Annotation of RNA Editing Sites

• Lee Soo-Youn

• Kim Ju-Han

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.1 27 ~ 32

• Genetics of Mitochondrial Myopathies

• Shin Jin-Hong

• Kim Dae-Seong

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.1 20 ~ 26

• Strategies for Mutation Discovery in Retinitis Pigmentosa: Transition to the Next Generation

• Yoo Chang-Ki

• Yu Hyeong-Gon

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.1 13 ~ 19

• Familial Juvenile Hyperuricemic Nephropathy and Uromodulin Gene Mutation

• Lee Young-Ki

• Lee Dong-Hun, Noh Jung-Woo

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.1 7 ~ 12

• Chronic Granulomatous Disease on Jeju Island, Korea

• Cho Moon-Jae

• Shin Kyung-Sue

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.1 1 ~ 6