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Prognostic indicators for long‐term outcome of non‐immune hydrops fetalis

Ultrasound in obstetrics & gynecology, 2024-04, Vol.63 (4), p.573-574

2024

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Maternal diabetes as a teratogenic factor in fetal congenital heart disease: more than hyperglycemia

Ultrasound in obstetrics & gynecology, 2024-03, Vol.63 (3), p.426-427

2024

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Born small‐for‐gestational age: not just smaller

Ultrasound in obstetrics & gynecology, 2023-09, Vol.62 (3), p.449-450

2023

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Role of late first‐trimester ultrasound in women with a positive NIPT result

Ultrasound in obstetrics & gynecology, 2023-10, Vol.62 (4), p.611-612

2023

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Is it time to adopt universal cytomegalovirus screening with valacyclovir prophylaxis in pregnancy?

Ultrasound in obstetrics & gynecology, 2023-01, Vol.61 (1), p.121-123

2023

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Outcomes associated with isolated agenesis of the corpus callosum diagnosed in utero

Ultrasound in obstetrics & gynecology, 2022-10, Vol.60 (4), p.587-588

2022

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Whole‐genome sequencing: is it appropriate in prenatal setting?

Ultrasound in obstetrics & gynecology, 2024-05, Vol.63 (5), p.705-706

2024

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NSF‐related fetal anemia and hydrops: new entity?

Ultrasound in obstetrics & gynecology, 2024-03, Vol.63 (3), p.421-422

2024

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Does chorionic villus sampling protect against fetal loss in twin pregnancy at high background risk of spontaneous miscarriage?

Ultrasound in obstetrics & gynecology, 2022-02, Vol.59 (2), p.273-274

2022

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Prenatal genetic evaluation of fetuses with structural anomaly: is it time to shift from microarray to exome sequencing as a first‐tier test?

Ultrasound in obstetrics & gynecology, 2023-01, Vol.61 (1), p.119-120

2023

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Ongoing reanalysis of prenatal exome sequencing data leads to higher diagnostic yield

Ultrasound in obstetrics & gynecology, 2022-06, Vol.59 (6), p.833-834

2022

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Perinatal outcome of late‐onset fetal growth restriction: etiology matters

Ultrasound in obstetrics & gynecology, 2022-11, Vol.60 (5), p.707-708

2022

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Fetal macrocephaly in late pregnancy: don't forget overgrowth syndromes

Ultrasound in obstetrics & gynecology, 2023-12, Vol.62 (6), p.908-909

2023

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Beyond diagnostic yield: use of exome sequencing in prenatal diagnosis

Ultrasound in obstetrics & gynecology, 2022-05, Vol.59 (5), p.697-698

2022

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Rare autosomal trisomies on non‐invasive prenatal testing: not as adverse as expected

Ultrasound in obstetrics & gynecology, 2019-12, Vol.54 (6), p.838-839

2019

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Prenatal diagnosis of non‐immune hydrops fetalis: whole‐exome sequencing or whole‐genome sequencing?

Ultrasound in obstetrics & gynecology, 2022-10, Vol.60 (4), p.585-586

2022

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Prenatal DNA diagnosis of Noonan syndrome in a fetus with increased nuchal translucency using next-generation sequencing

European journal of obstetrics & gynecology and reproductive biology, 2016-06, Vol.201, p.229-230

2016

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Screening for common β-globin gene cluster deletions in Chinese individuals with increased hemoglobin F

International journal of laboratory hematology, 2015-12, Vol.37 (6), p.752-757

2015

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Uptake of non-invasive prenatal testing in Chinese women: money matters

European journal of obstetrics & gynecology and reproductive biology, 2015-12, Vol.195, p.100-102

2015

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Study on JNK/AP-1 signaling pathway of airway mucus hypersecretion of severe pneumonia under RSV infection

European review for medical and pharmacological sciences, 2016-03, Vol.20 (5), p.853

2016

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Is there a nuchal translucency threshold above which biochemistry is unnecessary for 1st trimester screening in the Chinese population?

Journal of obstetrics and gynaecology, 2013-04, Vol.33 (3), p.280-281

2013

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Prenatal diagnosis of sex chromosome aneuploidies: experience at a mainland Chinese hospital

Journal of obstetrics and gynaecology, 2013-11, Vol.33 (8), p.827-829

2013

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Heterozygous β-thalassemia with complete absence of hemoglobin A2 in a Chinese adult

International journal of laboratory hematology, 2015-12, Vol.37 (6), p.e147-e149

2015

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Hb A2 levels in patients with nondeletional Hb H disease

International journal of laboratory hematology, 2012-12, Vol.34 (6), p.663-664

2012

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Acrania associated with amniotic bands in a fetus

Journal of obstetrics and gynaecology, 2012-05, Vol.32 (4), p.397-398

2012

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Prognostic indicators for long‐term outcome of non‐immune hydrops fetalis

Maternal diabetes as a teratogenic factor in fetal congenital heart disease: more than hyperglycemia

Born small‐for‐gestational age: not just smaller

Role of late first‐trimester ultrasound in women with a positive NIPT result

Is it time to adopt universal cytomegalovirus screening with valacyclovir prophylaxis in pregnancy?

Outcomes associated with isolated agenesis of the corpus callosum diagnosed in utero

Whole‐genome sequencing: is it appropriate in prenatal setting?

NSF‐related fetal anemia and hydrops: new entity?

Does chorionic villus sampling protect against fetal loss in twin pregnancy at high background risk of spontaneous miscarriage?

Prenatal genetic evaluation of fetuses with structural anomaly: is it time to shift from microarray to exome sequencing as a first‐tier test?

Ongoing reanalysis of prenatal exome sequencing data leads to higher diagnostic yield

Perinatal outcome of late‐onset fetal growth restriction: etiology matters

Fetal macrocephaly in late pregnancy: don't forget overgrowth syndromes

Beyond diagnostic yield: use of exome sequencing in prenatal diagnosis

Rare autosomal trisomies on non‐invasive prenatal testing: not as adverse as expected

Prenatal diagnosis of non‐immune hydrops fetalis: whole‐exome sequencing or whole‐genome sequencing?

Prenatal DNA diagnosis of Noonan syndrome in a fetus with increased nuchal translucency using next-generation sequencing

Screening for common β-globin gene cluster deletions in Chinese individuals with increased hemoglobin F

Uptake of non-invasive prenatal testing in Chinese women: money matters

Study on JNK/AP-1 signaling pathway of airway mucus hypersecretion of severe pneumonia under RSV infection

Is there a nuchal translucency threshold above which biochemistry is unnecessary for 1st trimester screening in the Chinese population?

Prenatal diagnosis of sex chromosome aneuploidies: experience at a mainland Chinese hospital

Heterozygous β-thalassemia with complete absence of hemoglobin A2 in a Chinese adult

Hb A2 levels in patients with nondeletional Hb H disease

Acrania associated with amniotic bands in a fetus

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