Browsing "Journal Papers" by Journal : Journal of genetic medicine
Showing results 12 to 25 of 25
| Pub Year | | Title | Author(s) |
| 2007 | | Development of medical genetics training program and certification process for medical geneticist as a specialist in Korea | 김현주 |
| 2015 | | Diagnostic approach for genetic causes of intellectual disability. | 임신영 |
| 2016 | | DNA damage to human genetic disorders with neurodevelopmental defects. | 이영수 |
| 2007 | | Genetic counseling in Korean health care system | 김현주 |
| 2013 | | Height and Bone Phenotype of 22q11.2 Deletion Syndrome: Lessons from the Gene Analysis of Three Cases | 손영배, 임신영, 정윤석 |
| 2013 | | Low-frequency Mosaicism of Trisomy 14, Missed by Array CGH | 손영배 |
| 2008 | | Molecular diagnosis of fragile X syndrome in a female child | 김현주, 정선용 |
| 2007 | | National survey for genetic counseling and demands for Professional genetic counselor | 김현주, 정윤석 |
| 2010 | | Phenotypic and Cytogenetic Delineation of Six Korean Children with Kabuki Syndrome | 고정민, 김현주 |
| 2012 | | Risk Reducing Surgery in Carriers with Double Heterozygosity for BRCA1 and BRCA2 Mutations | 강두경, 강석윤, 김구상, 김태희, 박명철, 임현이, 장석준, 전미선, 정용식, 홍우성 |
| 2007 | | Spinocerebellar ataxia 7 (SCA7) | 김현주, 정선용 |
| 2016 | | Substrate reduction therapy as a new treatment option for patients with Gaucher disease type 1: A review of literatures. | 손영배 |
| 2007 | | The spectrum of 5p deletion in Korean 20 patients with Cri du chat syndrome | 김현주 |
| 2011 | | Two Children with Saethre-Chotzen Syndrome Confirmed by the TWIST1 Gene Analysis | 윤수한, 정선용 |
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