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MeSH:(Gene Conversion)

1.The value of code conversion of human genome in medicine

Le Van Dong

Journal of Medical and Pharmaceutical Information 2004;0(7):9-16

2.Duplication and deletion of 21 hydroxylase gene among the normal Korean subjects and in adrenogenital syndrome patients.

Dong Kyu JIN ; Nam Seon BECK ; Phil Soo OH

Journal of Genetic Medicine 1997;1(1):27-32

3.Study of SMN gene in Chinese children with spinal muscular atrophy.

Wei-Liang LIU ; Fang LI ; Hong-Wei MA ; Hai-Yan LI

Chinese Journal of Contemporary Pediatrics 2010;12(7):539-543

4.CYP21A2 Mutation Analysis in Korean Patients With Congenital Adrenal Hyperplasia Using Complementary Methods: Sequencing After Long-Range PCR and Restriction Fragment Length Polymorphism Analysis With Multiple Ligation-Dependent Probe Amplification Assay.

Geehay HONG ; Hyung Doo PARK ; Rihwa CHOI ; Dong Kyu JIN ; Jae Hyeon KIM ; Chang Seok KI ; Soo Youn LEE ; Junghan SONG ; Jong Won KIM

Annals of Laboratory Medicine 2015;35(5):535-539

5.Molecular Diagnosis of 21-hydroxylase (CYP21) Gene mutations in Congenital Adrenal Hyperplasia.

Hyoung Song LEE ; Kang Woo CHEON ; Yong Seog PARK ; In Kwon HAN ; Inn Soo KANG

Korean Journal of Obstetrics and Gynecology 2001;44(6):1171-1177

6.Analysis of survival motor neuron gene conversion in patients with spinal muscular atrophy.

Sheng-xi HE ; Xiu-shan GE ; Yu-jin QU ; Yu-wei JIN ; Hong WANG ; Jin-li BAI ; Fang SONG

Chinese Journal of Medical Genetics 2011;28(6):606-611

7.Correlation between Genotype and Phenotype in Korean patients with Spinal Muscular Atrophy.

Seon Young WON ; Kyong Hwa RYU ; Eun Ha LEE ; Si Houn HAHN ; Ki Soo PAI ; Sung Hwan KIM

Journal of the Korean Child Neurology Society 1999;7(1):10-20

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