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Characteristics of incineration ash for sustainable treatment and reutilization

Environmental science and pollution research international, 2019-06, Vol.26 (17), p.16974-16997

2019

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Outcome of survivors with hemoglobin Bart's hydrops fetalis syndrome: The most severe form of α‐thalassemia

Pediatric transplantation, 2021-11, Vol.25 (7), p.e14090-n/a

2021

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Co‐occurrence of two rare genetic diseases: A potential pitfall for prenatal diagnosis in successive pregnancies

Prenatal diagnosis, 2020-12, Vol.40 (12), p.1606-1609

2020

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A novel MED12 pathogenic variant in a female fetus with facial cleft and cardiac defects identified in the first trimester

Prenatal diagnosis, 2024-07, Vol.44 (8), p.999-1002

2024

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Rapid prenatal diagnosis of skeletal dysplasia using medical trio exome sequencing: Benefit for prenatal counseling and pregnancy management

Prenatal diagnosis, 2020-04, Vol.40 (5), p.577-584

2020

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Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency

Prenatal diagnosis, 2020-10, Vol.40 (11), p.1426-1431

2020

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Prenatal exome sequencing in fetuses with callosal anomalies

Prenatal diagnosis, 2022-05, Vol.42 (6), p.744-752

2022

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Early prenatal diagnosis of hemoglobinopathy via celocentesis: Is it ready for use in routine clinical practice?

International journal of laboratory hematology, 2023-02, Vol.45 (1), p.e17-e18

2023

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All‐trans‐retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathway

Journal of cellular biochemistry, 2020-11, Vol.121 (11), p.4386-4396

2020

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Prenatal diagnosis of autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants presented with thick nuchal translucency and cardiac abnormalities

Prenatal diagnosis, 2023-12, Vol.43 (13), p.1662-1665

2023

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Whole‐exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography

Prenatal diagnosis, 2020-09, Vol.40 (10), p.1290-1299

2020

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Prenatal phenotypic discordance in monozygotic twins due to a postzygotic TSC2 variant

Prenatal diagnosis, 2021-01, Vol.41 (2), p.207-209

2021

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Prenatal diagnosis of X-linked hydrocephalus: The “hydrocephalus” is the focus

Taiwanese journal of obstetrics & gynecology, 2023-03, Vol.62 (2), p.380-381

2023

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Parental germline mosaic transmission of 5p13.2 microduplication in two siblings of a Chinese family

Journal of obstetrics and gynaecology, 2022-05, Vol.42 (4), p.701-703

2022

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Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease

Human genetics, 2021-02, Vol.140 (2), p.333-348

2021

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High accuracy of single‐molecule real‐time sequencing in detecting a rare α‐globin fusion gene in carrier screening population

Annals of human genetics, 2023-03, Vol.87 (1-2), p.9-17

2023

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Identification of thalassemia gene cluster deletion by long‐read whole‐genome sequencing (LR‐WGS)

International journal of laboratory hematology, 2021-08, Vol.43 (4), p.859-865

2021

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Secondary findings in prenatal exome sequencing: Ethical and counseling challenges

Taiwanese journal of obstetrics & gynecology, 2022-07, Vol.61 (4), p.728-729

2022

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α‐Haemoglobin pool measurement: a useful biomarker for evaluation of β‐thalassaemia intermedia?

British journal of haematology, 2018-11, Vol.183 (4), p.673-674

2018

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Prenatal diagnosis of Coffin‐Siris syndrome: What are the fetal features?

Prenatal diagnosis, 2022-11, Vol.42 (12), p.1488-1492

2022

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Pitfall in genetic screening in a pregnancy involving an allogeneic hematopoietic stem cell transplantation recipient

Prenatal diagnosis, 2019-01, Vol.39 (1), p.52-53

2019

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Germline mosaicism in an α‐thalassemia family: Incidental identification by prenatal ultrasound

Prenatal diagnosis, 2019-11, Vol.39 (12), p.1166-1169

2019

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Carnitine palmitoyltransferase II deficiency in a prenatal case with polycystic kidney disease‐like phenotype

Congenital anomalies, 2020-07, Vol.60 (4), p.131-132

2020

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Application of real‐time PCR–based multicolor melting curve with automatic analysis system in pregestational and prenatal thalassemia diagnoses

Annals of human genetics, 2023-11, Vol.87 (6), p.316-325

2023

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Idiopathic polyhydramnios and foetal macrosomia in the absence of maternal diabetes: clinical vigilance for costello syndrome

Journal of obstetrics and gynaecology, 2022-05, Vol.42 (4), p.704-706

2022

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Characteristics of incineration ash for sustainable treatment and reutilization

Outcome of survivors with hemoglobin Bart's hydrops fetalis syndrome: The most severe form of α‐thalassemia

Co‐occurrence of two rare genetic diseases: A potential pitfall for prenatal diagnosis in successive pregnancies

A novel MED12 pathogenic variant in a female fetus with facial cleft and cardiac defects identified in the first trimester

Rapid prenatal diagnosis of skeletal dysplasia using medical trio exome sequencing: Benefit for prenatal counseling and pregnancy management

Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency

Prenatal exome sequencing in fetuses with callosal anomalies

Early prenatal diagnosis of hemoglobinopathy via celocentesis: Is it ready for use in routine clinical practice?

All‐trans‐retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathway

Prenatal diagnosis of autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants presented with thick nuchal translucency and cardiac abnormalities

Whole‐exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography

Prenatal phenotypic discordance in monozygotic twins due to a postzygotic TSC2 variant

Prenatal diagnosis of X-linked hydrocephalus: The “hydrocephalus” is the focus

Parental germline mosaic transmission of 5p13.2 microduplication in two siblings of a Chinese family

Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease

High accuracy of single‐molecule real‐time sequencing in detecting a rare α‐globin fusion gene in carrier screening population

Identification of thalassemia gene cluster deletion by long‐read whole‐genome sequencing (LR‐WGS)

Secondary findings in prenatal exome sequencing: Ethical and counseling challenges

α‐Haemoglobin pool measurement: a useful biomarker for evaluation of β‐thalassaemia intermedia?

Prenatal diagnosis of Coffin‐Siris syndrome: What are the fetal features?

Pitfall in genetic screening in a pregnancy involving an allogeneic hematopoietic stem cell transplantation recipient

Germline mosaicism in an α‐thalassemia family: Incidental identification by prenatal ultrasound

Carnitine palmitoyltransferase II deficiency in a prenatal case with polycystic kidney disease‐like phenotype

Application of real‐time PCR–based multicolor melting curve with automatic analysis system in pregestational and prenatal thalassemia diagnoses

Idiopathic polyhydramnios and foetal macrosomia in the absence of maternal diabetes: clinical vigilance for costello syndrome

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