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| 1 |
Hereditary Breast Cancer in Korea
Kim, Sung-Won;
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Korean Society of Medical Genetics and Genomics
, v.9, no.1, pp.1-10,
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| 2 |
Application of Hot Start PCR Method in PCR-based Preimplantation Genetic Diagnosis
Kim, Sung-Ah;Kang, Moon-Joo;Kim, Hee-Sun;Oh, Sun-Kyung;Ku, Seung-Yup;Choi, Young-Min;Jun, Jong-Kwan;Moon, Shin-Yong;
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Korean Society of Medical Genetics and Genomics
, v.9, no.1, pp.11-16,
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| 3 |
Analysis of Parental Decisions Based on Sex Chromosome Abnormalities Detected Prenatally: A Ten-year update (2001-2010)
An, Gye-Hyeong;Choi, Kyu-Hong;Yang, Jae-Hyug;Kim, Moon-Young;Han, Jung-Yeol;Park, So-Yeon;Lee, Bom-Yi;Lee, Da-Eun;Ryu, Hyun-Mee;
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Korean Society of Medical Genetics and Genomics
, v.9, no.1, pp.17-21,
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| 4 |
Fetal Loss Rate after Mid-trimester Amniocentesis
Han, You-Jung;Kim, Yun-Young;Lee, Si-Won;Kim, Min-Hyoung;Chung, Jin-Hoon;Ahn, Hyun-Kyong;Han, Jung-Yeol;Kim, Moon-Young;Yang, Jae-Hyug;Choi, Kyu-Hong;Park, So-Yeon;Ryu, Hyun-Mee;
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Korean Society of Medical Genetics and Genomics
, v.9, no.1, pp.22-24,
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| 5 |
Risk Reducing Surgery in Carriers with Double Heterozygosity for BRCA1 and BRCA2 Mutations
Hong, Woo-Sung;Kim, Ku-Sang;Jung, Yong-Sik;Kang, Seok-Yun;Kang, Doo-Kyoung;Kim, Tae-Hee;Yim, Hyunee;Chun, Mi-Son;Park, Myong-Chul;Chang, Suk-Joon;
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Korean Society of Medical Genetics and Genomics
, v.9, no.1, pp.25-30,
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| 6 |
A Case with Spondyloepiphyseal Dysplasia Tarda with TRAPPC2 Mutation
Kim, Hyun-Jin;Lee, Beom-Hee;Kim, Yoo-Mi;Kim, Gu-Hwan;Kim, Ok-Hwa;Yoo, Han-Wook;
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Korean Society of Medical Genetics and Genomics
, v.9, no.1, pp.31-34,
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| 7 |
A Case with Emanuel Syndrome Resulting from a Maternal Balanced Translocation
Kim, Ja-Hye;Kim, Yoo-Mi;Lee, Beom-Hee;Kim, Ja-Hyung;Seo, Eul-Ju;Yoo, Han-Wook;
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Korean Society of Medical Genetics and Genomics
, v.9, no.1, pp.35-37,
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| 8 |
A Korean Family with Cholesterol Ester Transfer Protein Deficiency
Youn, Seo-Young;Shin, Ik-Soon;Hong, Yong-Hee;Lee, Dong-Hwan;
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Korean Society of Medical Genetics and Genomics
, v.9, no.1, pp.38-41,
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| 9 |
Identification of Novel Compound Heterozygous Mutations in the ACADS Gene of an Asymptomatic Korean Newborn with Short Chain Acyl-CoA Dehydrogenase Deficiency by Tandem Mass Spectrometry
Cheon, Chong-Kun;Choi, Hyung-Soon;Kim, Su-Yung;Yoo, Han-Wook;Kim, Gu-Hwan;
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Korean Society of Medical Genetics and Genomics
, v.9, no.1, pp.42-46,
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