Fang-yu Hung

Hsinchu, TNQ, Taiwan

Last Updated: 09/26/2026

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Found 12 publications

Dengue Epidemiology in 7 Southeast Asian Countries: 24-Year, Retrospective, Multicountry Ecological Study.

Dengue Epidemiology in 7 Southeast Asian Countries: 24-Year, Retrospective, Multicountry Ecological Study.

Journal: Interactive journal of medical research

Published: December 24, 2024

Molecular cytogenetic characterization of de novo concomitant distal 8p deletion of 8p23.3p23.1 and Xp and Xq deletion of Xp22.13q28 due to an unbalanced X;8 translocation detected by amniocentesis.

Molecular cytogenetic characterization of de novo concomitant distal 8p deletion of 8p23.3p23.1 and Xp and Xq deletion of Xp22.13q28 due to an unbalanced X;8 translocation detected by amniocentesis.

Journal: Taiwanese journal of obstetrics & gynecology

Published: January 07, 2022

iDPGK: characterization and identification of lysine phosphoglycerylation sites based on sequence-based features.

iDPGK: characterization and identification of lysine phosphoglycerylation sites based on sequence-based features.

Journal: BMC bioinformatics

Published: August 10, 2020

Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome.

Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome.

Journal: Taiwanese journal of obstetrics & gynecology

Published: September 06, 2019

Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound.

Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound.

Journal: Taiwanese journal of obstetrics & gynecology

Published: October 17, 2017

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2.

Journal: Taiwanese journal of obstetrics & gynecology

Published: January 12, 2017

Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome.

Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome.

Journal: Taiwanese journal of obstetrics & gynecology

Published: January 12, 2017

Genome-wide discovery of viral microRNAs based on phylogenetic analysis and structural evolution of various human papillomavirus subtypes.

Genome-wide discovery of viral microRNAs based on phylogenetic analysis and structural evolution of various human papillomavirus subtypes.

Journal: Briefings in bioinformatics

Published: December 04, 2016

Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome.

Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome.

Journal: Taiwanese journal of obstetrics & gynecology

Published: August 30, 2016

Preoperative measurement of maternal abdominal circumference relates the initial sensory block level of spinal anesthesia for cesarean section: An observational study.

Preoperative measurement of maternal abdominal circumference relates the initial sensory block level of spinal anesthesia for cesarean section: An observational study.

Journal: Taiwanese journal of obstetrics & gynecology

Published: April 07, 2015

Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony.

Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony.

Journal: Taiwanese journal of obstetrics & gynecology

Published: March 28, 2013

Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II.

Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II.

Journal: Taiwanese journal of obstetrics & gynecology

Published: February 17, 2012

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Last Updated: 09/26/2026