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| 1 |
Modeling of Human Genetic Diseases Via Cellular, Reprogramming
Kang, Min-Yong;Suh, Ji-Hoon;Han, Yong-Mahn;
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Korean Society of Medical Genetics and Genomics
, v.9, no.2, pp.67-72,
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| 2 |
Prenatal Population Screening for Fragile X Carrier and the Prevalence of Premutation Carriers in, Korea
Han, Sung-Hee;Heo, Yun-Ah;Yang, Young-Ho;Kim, Young-Jin;Cho, Han-Ik;Lee, Kyoung-Ryul;
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Korean Society of Medical Genetics and Genomics
, v.9, no.2, pp.73-77,
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| 3 |
Maternal Plasma Hepatocyte Growth Factor Concentrations in Women Who Subsequently Developed Preeclampsia
Kim, Shin Young;Park, So Yeon;Kim, Mi Jin;Kim, Moon Young;Choi, Kyu Hong;Kwak, Dong Wook;Han, Yoo Jung;Ryu, Hyun Mee;
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Korean Society of Medical Genetics and Genomics
, v.9, no.2, pp.78-83,
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| 4 |
Correlation Between Unidentified Bright Objects on Brain Magnetic Resonance Imaging (MRI) and Cerebral Glucose Metabolism in Patients with Neurofibromatosis Type 1
Sohn, Young Bae;An, Young Sil;Lee, Su Jin;Choi, Jin Wook;Jeong, Seon-Yong;Kim, Hyon-Ju;Ko, Jung Min;
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Korean Society of Medical Genetics and Genomics
, v.9, no.2, pp.84-88,
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| 5 |
A Korean Girl with Campomelic Dysplasia caused by a Novel Nonsense Mutation within the SOX9 Gene
Ko, Jung Min;Hah, J.-Hun;Kim, Suk-Wha;Cho, Tae-Joon;Kim, Gu-Hwan;Yoo, Han-Wook;
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Korean Society of Medical Genetics and Genomics
, v.9, no.2, pp.89-92,
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| 6 |
A Korean Patient with Kniest Syndrome associated with Lipomeningomyelocele
Min, Hye Won;Koo, Kyo Yeon;Lee, Chul Ho;Yang, Jeong Yoon;Lee, Jin-Sung;
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Korean Society of Medical Genetics and Genomics
, v.9, no.2, pp.93-97,
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| 7 |
A Familial Case with Holt-Oram Syndrome with a Novel TBX5 Mutation
Lee, Beom Hee;Kim, Yoo-Mi;Kim, Gu-Hwan;Kim, Young-Hwue;Yoo, Han-Wook;
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Korean Society of Medical Genetics and Genomics
, v.9, no.2, pp.98-100,
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| 8 |
A Prenatal Case of Paracentric Inversion of Chromosome 18, inv(18)(q21.1q22)
An, Gye-Hyeong;Kim, Moon Young;Kim, Min Hyoung;Kim, Yun Young;Choi, Kyu Hong;Kwak, Dong Wook;Park, So Yeon;Lee, Bom Yi;Park, Ju Yeon;Ryu, Hyun Mee;
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Korean Society of Medical Genetics and Genomics
, v.9, no.2, pp.101-103,
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