J. Kim

发表

Detection of cryptic Y chromosome mosaicism by coamplification PCR with archived cytogenetic slides of suspected Turner syndrome

S. Y. Park, J. Han, Young Mi Kim, 2000, Experimental & Molecular Medicine.

Three cases of rare SRY-negative 46,XX testicular disorder of sexual development with complete masculinization and a review of the literature

S. Y. Park, J. Seo, H. Ryu, 2016 .

Association between genetic polymorphisms in folate-related enzyme genes and infertile men with non-obstructive azoospermia

S. Y. Park, J. Seo, Shin-Young Kim, 2015, Systems biology in reproductive medicine.

Prenatally Diagnosed Uncommon Mosaic Autosomal Trisomy

S. Y. Park, H. Ryu, B. Lee, 2009 .

Evaluation of extraction methods for methylated cell-free fetal DNA from maternal plasma

S. Y. Park, D. Kwak, H. Ryu, 2018, Journal of Assisted Reproduction and Genetics.

Duplication of intrachromosomal insertion segments 4q32→q35 confirmed by comparative genomic hybridization and fluorescent in situ hybridization

S. Y. Park, M. Koong, I. Kang, 2011, Clinical and Experimental Reproductive Medicine.

Chromosomal Abnormalities in Korean Fetuses with Nuchal Translucency above the 99th Percentile

Eun Hye Chang, D. Kwak, H. Boo, 2019, Perinatology.

Reduced Number of Endothelial Progenitor Colony-Forming Units in Patients with Preeclampsia

S. Y. Park, J. Han, H. Ahn, 2010 .

Klinefelter Syndrome Diagnosed by Prenatal Screening Tests in High-Risk Groups

S. Y. Park, J. Seo, Joong Shik Lee, 2013, Korean journal of urology.

Epigenome-wide base-resolution profiling of DNA methylation in chorionic villi of fetuses with Down syndrome by methyl-capture sequencing

H. Ryu, Moon-Young Kim, J. Chung, 2019, Clinical Epigenetics.

Effective Fetal Epigenetic Biomarkers for Noninvasive Fetal Trisomy 21 Detections

J. Han, H. Ryu, Moon-Young Kim, 2018, Fetal Diagnosis and Therapy.