Se R. Sung

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 11 publications

Exome sequencing for the patients with SRY-negative 46,XX testicular disorder of sex development.

Exome sequencing for the patients with SRY-negative 46,XX testicular disorder of sex development.

Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: August 05, 2020

The association of stromal antigen 3 (STAG3) sequence variations with spermatogenic impairment in the male Korean population.

The association of stromal antigen 3 (STAG3) sequence variations with spermatogenic impairment in the male Korean population.

Journal: Asian journal of andrology
Published: May 23, 2019

Neurodegeneration in an adolescent with Sjogren-Larsson syndrome: a decade-long follow-up case report.

Neurodegeneration in an adolescent with Sjogren-Larsson syndrome: a decade-long follow-up case report.

Journal: BMC medical genetics
Published: May 25, 2018

Impact of RFC1, MTHFR, and MTHFD1 polymorphism on unexplained pregnancy loss (UPL): comparative analysis of maternal and fetal components using mother-abortus paired samples.

Impact of RFC1, MTHFR, and MTHFD1 polymorphism on unexplained pregnancy loss (UPL): comparative analysis of maternal and fetal components using mother-abortus paired samples.

Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: April 30, 2018

Sequence variations of the EGR4 gene in Korean men with spermatogenesis impairment.

Sequence variations of the EGR4 gene in Korean men with spermatogenesis impairment.

Journal: BMC medical genetics
Published: April 19, 2016

Analysis of the cell-free amniotic fluid transcriptome expressed during the euploid mid-trimester of pregnancy.

Analysis of the cell-free amniotic fluid transcriptome expressed during the euploid mid-trimester of pregnancy.

Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: February 25, 2016

Molecular genetic and cytogenetic characterization of a partial Xp duplication and Xq deletion in a patient with premature ovarian failure.

Molecular genetic and cytogenetic characterization of a partial Xp duplication and Xq deletion in a patient with premature ovarian failure.

Journal: Gene
Published: June 11, 2013

Molecular analysis of miscarriage products using multiplex ligation-dependent probe amplification (MLPA): alternative to conventional karyotype analysis.

Molecular analysis of miscarriage products using multiplex ligation-dependent probe amplification (MLPA): alternative to conventional karyotype analysis.

Journal: Archives of gynecology and obstetrics
Published: May 28, 2013

Gene expression analysis of the microdissected trophoblast layer of human placenta after the spontaneous onset of labor.

Gene expression analysis of the microdissected trophoblast layer of human placenta after the spontaneous onset of labor.

Journal: PloS one
Published: May 28, 2013

Genome-wide screening of severe male factor infertile patients using BAC-array comparative genomic hybridization (CGH).

Genome-wide screening of severe male factor infertile patients using BAC-array comparative genomic hybridization (CGH).

Journal: Gene
Published: February 21, 2012

Impaired spermatogenesis and gr/gr deletions related to Y chromosome haplogroups in Korean men.

Impaired spermatogenesis and gr/gr deletions related to Y chromosome haplogroups in Korean men.

Journal: PloS one
Published: February 07, 2012
Showing 1-11 of 11

Last Updated: 09/26/2026