Shih-ting Y. Lai
TPQ, Taiwan
Last Updated: 09/26/2026
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Found 41 publications
The correlation with abnormal fetal outcome and a high level of amniotic fluid alpha-fetoprotein in mid-trimester.
Journal: Taiwanese journal of obstetrics & gynecology
Published: December 26, 2022
Prenatal diagnosis of persistent left superior vena cava, polyhydramnios and a small gastric bubble in a fetus with VACTERL association.
Journal: Taiwanese journal of obstetrics & gynecology
Published: March 12, 2020
Monozygotic twins discordant for low-level mosaic trisomy 17 at amniocentesis in a pregnancy with a favorable outcome and a literature review of heterokaryotypic monozygotic twins at amniocentesis.
Journal: Taiwanese journal of obstetrics & gynecology
Published: December 19, 2019
Reply to Comment on An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus.
Journal: Journal of medical ultrasound
Published: October 05, 2018
An Intrauterine Gestational sac Surrounded by Thin Myometrium at Fundus.
Journal: Journal of medical ultrasound
Published: August 02, 2018
An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus.
Journal: Journal of medical ultrasound
Published: August 02, 2018
First-trimester cystic hygroma and omphalocele in a fetus with Turner syndrome.
Journal: Taiwanese journal of obstetrics & gynecology
Published: May 30, 2018
Detection of hypomethylation of H19 in a pregnancy with limb-body wall complex.
Journal: Taiwanese journal of obstetrics & gynecology
Published: May 30, 2018
Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound.
Journal: Taiwanese journal of obstetrics & gynecology
Published: May 30, 2018
Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.
Journal: Taiwanese journal of obstetrics & gynecology
Published: May 30, 2018
Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1 and PAFAH1B1 in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and developmental delay.
Journal: Taiwanese journal of obstetrics & gynecology
Published: May 30, 2018
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.
Journal: Taiwanese journal of obstetrics & gynecology
Published: May 30, 2018
Last Updated: 09/26/2026