Hongmei Zhu

17 South Renmin Road
Chengdu, China

Last Updated: 09/26/2026

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Found 28 publications

Evaluating the clinical utility and strategy of whole-exome sequencing testing for fetuses with increased nuchal translucency.

Evaluating the clinical utility and strategy of whole-exome sequencing testing for fetuses with increased nuchal translucency.

Journal: American journal of obstetrics and gynecology

Published: February 21, 2025

Effect of 18F-DCFPyL PET on changes in management of patients with prostate cancer: a systematic review and meta-analysis.

Effect of 18F-DCFPyL PET on changes in management of patients with prostate cancer: a systematic review and meta-analysis.

Journal: Frontiers in medicine

Published: December 13, 2023

A prenatal case misunderstood as specimen confusion: 46,XY/46,XY chimerism.

A prenatal case misunderstood as specimen confusion: 46,XY/46,XY chimerism.

Journal: BMC pregnancy and childbirth

Published: November 03, 2023

Prenatal prevalence and postnatal manifestations of 16p11.2 deletions: A new insights into neurodevelopmental disorders based on clinical investigations combined with multi-omics analysis.

Prenatal prevalence and postnatal manifestations of 16p11.2 deletions: A new insights into neurodevelopmental disorders based on clinical investigations combined with multi-omics analysis.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: June 08, 2023

A chromosomal microarray analysis-based laboratory algorithm for the detection of genetic etiology of early pregnancy loss.

A chromosomal microarray analysis-based laboratory algorithm for the detection of genetic etiology of early pregnancy loss.

Journal: Frontiers in genetics

Published: April 11, 2023

Defining the scope of extended NIPS in Western China: evidence from a large cohort of fetuses with normal ultrasound scans.

Defining the scope of extended NIPS in Western China: evidence from a large cohort of fetuses with normal ultrasound scans.

Journal: BMC pregnancy and childbirth

Published: March 10, 2023

Case report: A novel de novo deletion mutation of DYRK1A is associated with intellectual developmental disorder, autosomal dominant 7.

Case report: A novel de novo deletion mutation of DYRK1A is associated with intellectual developmental disorder, autosomal dominant 7.

Journal: Frontiers in neuroscience

Published: February 27, 2023

Case report: Prenatal diagnosis of rare chromosome mosaicism: discordant results between chorionic villi and amniotic fluid samples.

Case report: Prenatal diagnosis of rare chromosome mosaicism: discordant results between chorionic villi and amniotic fluid samples.

Journal: Frontiers in genetics

Published: February 24, 2023

Embryonic organizer formation disorder leads to multiorgan dysplasia in Down syndrome.

Embryonic organizer formation disorder leads to multiorgan dysplasia in Down syndrome.

Journal: Cell death & disease

Published: August 17, 2022

Case Report: Preimplantation Genetic Testing for X-Linked Severe Combined Immune Deficiency Caused by IL2RG Gene Variant.

Case Report: Preimplantation Genetic Testing for X-Linked Severe Combined Immune Deficiency Caused by IL2RG Gene Variant.

Journal: Frontiers in genetics

Published: April 22, 2022

Analysis of autosomal dominant genes impacted by copy number loss in 24,844 fetuses without structural abnormalities.

Analysis of autosomal dominant genes impacted by copy number loss in 24,844 fetuses without structural abnormalities.

Journal: BMC genomics

Published: October 14, 2021

Preimplantation Genetic Testing for Rare Inherited Disease of MMA-CblC: an Unaffected Live Birth.

Preimplantation Genetic Testing for Rare Inherited Disease of MMA-CblC: an Unaffected Live Birth.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: February 26, 2021

Showing 1-12 of 28

Last Updated: 09/26/2026