Jianzhu Wu

Shenzhen, China

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 18 publications

Prenatal diagnosis of fetuses with Emanuel syndrome: Results of ultrasound examination and invasive genetic testing.

Prenatal diagnosis of fetuses with Emanuel syndrome: Results of ultrasound examination and invasive genetic testing.

Journal: Prenatal diagnosis
Published: July 18, 2021

Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family.

Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family.

Journal: Frontiers in genetics
Published: December 13, 2020

Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletions.

Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletions.

Journal: Prenatal diagnosis
Published: December 14, 2017

Prenatal genetic analysis of two fetuses with Miller-Dieker syndrome

Prenatal genetic analysis of two fetuses with Miller-Dieker syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 11, 2017

An SNP panel for the analysis of paternally inherited alleles in maternal plasma using ion Torrent PGM.

An SNP panel for the analysis of paternally inherited alleles in maternal plasma using ion Torrent PGM.

Journal: International journal of legal medicine
Published: January 09, 2017

Application of single nucleotide polymorphism-based array analysis for prenatal diagnosis of a fetus with de novo derivative chromosome

Application of single nucleotide polymorphism-based array analysis for prenatal diagnosis of a fetus with de novo derivative chromosome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 01, 2016

Prenatal diagnosis of 1p36.3 microdeletion in a fetus with complex heart defect

Prenatal diagnosis of 1p36.3 microdeletion in a fetus with complex heart defect

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 07, 2016

Genetic analysis of a fetus with partial 1q monosomy and partial 17q trisomy

Genetic analysis of a fetus with partial 1q monosomy and partial 17q trisomy

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 07, 2016

Prenatal genetic diagnosis for a fetus with atypical neurofibromatosis type 1 microdeletion

Prenatal genetic diagnosis for a fetus with atypical neurofibromatosis type 1 microdeletion

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 10, 2016

Chromosomal microarray analysis for lateral ventriculomegaly in fetus

Chromosomal microarray analysis for lateral ventriculomegaly in fetus

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 15, 2015

Misdiagnosis of mosaic tetrasomy 9p in a fetus by single nucleotide polymorphism-based array

Misdiagnosis of mosaic tetrasomy 9p in a fetus by single nucleotide polymorphism-based array

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 15, 2015

Prenatal diagnosis of five cases of monochorionic-diamniotic twins discordant for karyotype analysis

Prenatal diagnosis of five cases of monochorionic-diamniotic twins discordant for karyotype analysis

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 30, 2015
Showing 1-12 of 18

Last Updated: 09/26/2026