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| 1 |
Whole genome sequencing based noninvasive prenatal test
Cho, Eun-Hae;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.61-65,
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| 2 |
Advantages of the single nucleotide polymorphism-based noninvasive prenatal test
Kim, Kunwoo;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.66-71,
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| 3 |
Application of digital polymerase chain reaction technology for noninvasive prenatal test
Lee, Seung Yong;Hwang, Seung Yong;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.72-78,
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| 4 |
Validation of fetus aneuploidy in 221 Korean clinical samples using noninvasive chromosome examination: Clinical laboratory improvement amendments-certified noninvasive prenatal test
Kim, Min-Jeong;Kwon, Chang Hyuk;Kim, Dong-In;Im, Hee Su;Park, Sungil;Kim, Ji Ho;Bae, Jin-Sik;Lee, Myunghee;Lee, Min Seob;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.79-84,
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| 5 |
Noninvasive prenatal test for fetal chromosomal aneuploidies by massively parallel sequencing of cell-free fetal DNA in maternal plasma: The first clinical experience in Korea
Han, Sung-Hee;Yang, Young-Ho;Ryu, Jae-Song;Kang, Myung-Soo;Kim, Young-Jin;Lee, Kyoung-Ryul;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.85-91,
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| 6 |
Observed frequency of fetal trisomy between 16 and 24 gestational weeks in pregnant women older than 34 years at delivery
Jeong, Shin Ok;Han, You Jung;Lee, Si Won;Kwak, Dong Wook;Chung, Jin Hoon;Ahn, Hyun Kyong;Choi, June Seek;Han, Jung Yeol;Kim, Moon Young;Park, So Yeon;Ryu, Hyun Mee;Kim, Min Hyoung;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.92-95,
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| 7 |
Evaluating the results of the Momguard noninvasive prenatal test
Hu, Hae-Jin;Kwon, Young-Jun;Oh, Mijin;Kim, Jihun;Cho, Dae-Yeon;Seo, Dong-Hee;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.96-99,
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| 8 |
Noninvasive fetal RHD genotyping using cell-free fetal DNA incorporating fetal RASSF1A marker in RhD-negative pregnant women in Korea
Han, Sung-Hee;Yang, Young-Ho;Ryu, Jae-Song;Kim, Young-Jin;Lee, Kyoung-Ryul;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.100-108,
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| 9 |
Identification of causative mutations in patients with Leigh syndrome and MERRF by mitochondrial DNA-targeted next-generation sequencing
Hong, Hyun Dae;Kim, Eunja;Nam, Soo Hyun;Yoo, Da Hye;Suh, Bum Chun;Choi, Byung-Ok;Chung, Ki Wha;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.109-117,
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| 10 |
Noninvasive prenatal test for the pregnancy with Turner syndrome mosaicism 45, X/47, XXX: A case report
Kim, Ji Hye;Lee, Gun Ho;Cha, Dong Hyun;Cho, Eun-Hae;Jung, Yong Wook;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.118-122,
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| 11 |
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: A prenatal diagnosis report
Cho, In Ae;Park, Ji Kwon;Baek, Jong Chul;Ha, A Na;Kang, Min Young;Lee, Jae Ik;Park, Ji Eun;Shin, Jeong Kyu;Choi, Won Jun;Lee, Soon Ae;Lee, Jong Hak;Paik, Won Young;
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Korean Society of Medical Genetics and Genomics
, v.12, no.2, pp.123-127,
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