Lv-yin G. Huang

Guangzhou, China

Last Updated: 09/26/2026

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Found 26 publications

Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency.

Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency.

Journal: Prenatal diagnosis
Published: February 02, 2020

Congenital Cystic Diaphragm with Diaphragmatic Eventration in a Fetus: A Case Presentation.

Congenital Cystic Diaphragm with Diaphragmatic Eventration in a Fetus: A Case Presentation.

Journal: Fetal and pediatric pathology
Published: March 27, 2019

Prenatal diagnosis of 17q12 deletion syndrome: a retrospective case series.

Prenatal diagnosis of 17q12 deletion syndrome: a retrospective case series.

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: January 13, 2019

Early prenatal detection of short-rib polydactyly syndrome in a monochorionic diamniotic twin pregnancy.

Early prenatal detection of short-rib polydactyly syndrome in a monochorionic diamniotic twin pregnancy.

Journal: Congenital anomalies
Published: August 03, 2018

Early prenatal diagnosis of 49,XXXXY: two case reports.

Early prenatal diagnosis of 49,XXXXY: two case reports.

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: June 10, 2018

δ-Thalassemia with Complete Absence of Hb A2 in a Chinese Family.

δ-Thalassemia with Complete Absence of Hb A2 in a Chinese Family.

Journal: Hemoglobin
Published: May 09, 2018

A cost-effectiveness analysis comparing two different strategies in advanced maternal age: Combined first-trimester screening and maternal blood cell-free DNA testing.

A cost-effectiveness analysis comparing two different strategies in advanced maternal age: Combined first-trimester screening and maternal blood cell-free DNA testing.

Journal: Taiwanese journal of obstetrics & gynecology
Published: May 03, 2018

Prenatal diagnosis of Wolf-Hirschhorn syndrome at the first trimester using chromosomal microarray analysis.

Prenatal diagnosis of Wolf-Hirschhorn syndrome at the first trimester using chromosomal microarray analysis.

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: April 11, 2018

Application of noninvasive prenatal testing in pregnancies with fetal double bubble sign: Is it feasible?

Application of noninvasive prenatal testing in pregnancies with fetal double bubble sign: Is it feasible?

Journal: Prenatal diagnosis
Published: March 26, 2018

Chromosomal microarray analysis detects trisomy 9 mosaicism in a prenatal case not revealed by conventional cytogenetic analysis of cord blood.

Chromosomal microarray analysis detects trisomy 9 mosaicism in a prenatal case not revealed by conventional cytogenetic analysis of cord blood.

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: March 22, 2018

What would be missed in the first trimester if nuchal translucency measurement is replaced by cell free DNA foetal aneuploidy screening?

What would be missed in the first trimester if nuchal translucency measurement is replaced by cell free DNA foetal aneuploidy screening?

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: February 13, 2018

Prenatal diagnosis of Wolf-Hirschhorn syndrome: Ultrasonography and molecular karyotyping results.

Prenatal diagnosis of Wolf-Hirschhorn syndrome: Ultrasonography and molecular karyotyping results.

Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: January 12, 2018
Showing 1-12 of 26

Last Updated: 09/26/2026