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The effects of spherical video-based virtual reality implementation on students' natural science learning effectiveness

Interactive learning environments, 2020-10, Vol.28 (7), p.915-929

2020

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Congenital radioulnar synostosis: is prenatal diagnosis possible? - A case report

Taiwanese journal of obstetrics & gynecology, 2023-03, Vol.62 (2), p.334-335

2023

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Prenatal Ultrasound Evaluation and Outcome of Pregnancy with Fetal Cystic Hygromas and Lymphangiomas

Journal of medical ultrasound, 2017-03, Vol.25 (1), p.12-15

2017

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Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound

Taiwanese journal of obstetrics & gynecology, 2018-10, Vol.57 (5), p.739-744

2018

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

Taiwanese journal of obstetrics & gynecology, 2017-04, Vol.56 (2), p.268-269

2017

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Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13 , ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency

Taiwanese journal of obstetrics & gynecology, 2017-06, Vol.56 (3), p.398-401

2017

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Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3

Taiwanese journal of obstetrics & gynecology, 2017-02, Vol.56 (1), p.87-92

2017

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Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction

Taiwanese journal of obstetrics & gynecology, 2016-06, Vol.55 (3), p.415-418

2016

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review

Taiwanese journal of obstetrics & gynecology, 2017-08, Vol.56 (4), p.554-557

2017

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Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review

Taiwanese journal of obstetrics & gynecology, 2016-10, Vol.55 (5), p.712-717

2016

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Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis

Taiwanese journal of obstetrics & gynecology, 2017-04, Vol.56 (2), p.230-233

2017

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Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound

Taiwanese journal of obstetrics & gynecology, 2017-02, Vol.56 (1), p.102-105

2017

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Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome

Taiwanese journal of obstetrics & gynecology, 2016-10, Vol.55 (5), p.745-747

2016

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An Intrauterine Gestational sac Surrounded by Thin Myometrium at Fundus

Journal of medical ultrasound, 2017-12, Vol.25 (4), p.255-257

2017

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Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion

Taiwanese journal of obstetrics & gynecology, 2016-10, Vol.55 (5), p.733-737

2016

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Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot

Taiwanese journal of obstetrics & gynecology, 2016-04, Vol.55 (2), p.270-274

2016

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Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication

Taiwanese journal of obstetrics & gynecology, 2016-08, Vol.55 (4), p.596-601

2016

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Prenatal Ultrasound Findings of Pregnancy Associated with Zika Virus Infection

Journal of medical ultrasound, 2016-09, Vol.24 (3), p.89-92

2016

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An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus

Journal of medical ultrasound, 2017-09, Vol.25 (3), p.188-189

2017

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Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability

Taiwanese journal of obstetrics & gynecology, 2016-12, Vol.55 (6), p.856-860

2016

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Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)

Taiwanese journal of obstetrics & gynecology, 2016-04, Vol.55 (2), p.288-292

2016

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Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling

Taiwanese journal of obstetrics & gynecology, 2016-12, Vol.55 (6), p.897-899

2016

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Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3–q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1 , RAD21 and EXT1

Taiwanese journal of obstetrics & gynecology, 2015-10, Vol.54 (5), p.592-596

2015

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Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly

Taiwanese journal of obstetrics & gynecology, 2016-08, Vol.55 (4), p.591-595

2016

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Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2–q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome

Taiwanese journal of obstetrics & gynecology, 2014-12, Vol.53 (4), p.583-587

2014

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The effects of spherical video-based virtual reality implementation on students' natural science learning effectiveness

Congenital radioulnar synostosis: is prenatal diagnosis possible? - A case report

Prenatal Ultrasound Evaluation and Outcome of Pregnancy with Fetal Cystic Hygromas and Lymphangiomas

Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound

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

Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13 , ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency

Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3

Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review

Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review

Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis

Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound

Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome

An Intrauterine Gestational sac Surrounded by Thin Myometrium at Fundus

Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion

Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot

Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication

Prenatal Ultrasound Findings of Pregnancy Associated with Zika Virus Infection

An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)

Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling

Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3–q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1 , RAD21 and EXT1

Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly

Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2–q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome

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