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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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不同合作學習模式結合遊戲式學習對小學生運算思維學習成效之影響

Chen, Yen-Ni

2019

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Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1 , NIPA2 , CYFIP1 , and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay

Taiwanese journal of obstetrics & gynecology, 2017-02, Vol.56 (1), p.93-97

2017

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Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review

Taiwanese journal of obstetrics & gynecology, 2015-08, Vol.54 (4), p.426-431

2015

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Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome

Taiwanese journal of obstetrics & gynecology, 2017-04, Vol.56 (2), p.238-242

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 low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome

Taiwanese journal of obstetrics & gynecology, 2016-12, Vol.55 (6), p.900-901

2016

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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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Recurrent 2q13 microduplication encompassing MALL , NPHP1 , RGPD6 , and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder

Taiwanese journal of obstetrics & gynecology, 2017-02, Vol.56 (1), p.98-101

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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Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes

Taiwanese journal of obstetrics & gynecology, 2016-04, Vol.55 (2), p.285-287

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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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 of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality

Taiwanese journal of obstetrics & gynecology, 2016-12, Vol.55 (6), p.871-873

2016

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

Taiwanese journal of obstetrics & gynecology, 2016-12, Vol.55 (6), p.902-903

2016

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Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome

Taiwanese journal of obstetrics & gynecology, 2016-04, Vol.55 (2), p.303-304

2016

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Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome

Taiwanese journal of obstetrics & gynecology, 2016-10, Vol.55 (5), p.728-732

2016

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

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

不同合作學習模式結合遊戲式學習對小學生運算思維學習成效之影響

Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1 , NIPA2 , CYFIP1 , and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay

Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome

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

Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome

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

Recurrent 2q13 microduplication encompassing MALL , NPHP1 , RGPD6 , and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder

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

Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes

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

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

Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality

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

Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome

Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome

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

An Intrauterine Gestational sac Surrounded by Thin Myometrium at Fundus

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

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

Prenatal Ultrasound Findings of Pregnancy Associated with Zika Virus Infection

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