Chuan Zhang

Key Laboratory Of Maternal Fetal Medicine And Reproductive Protection Of Gansu Province
Lanzhou, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

Prenatal genotype-phenotype correlations in four fetuses with Rubinstein-Taybi syndrome due to EP300 mutations: a case series and literature review.

Prenatal genotype-phenotype correlations in four fetuses with Rubinstein-Taybi syndrome due to EP300 mutations: a case series and literature review.

Journal: Frontiers in genetics

Published: April 28, 2026

Diagnosing fetal apert syndrome: a case study on prenatal diagnosis and genetic insights.

Diagnosing fetal apert syndrome: a case study on prenatal diagnosis and genetic insights.

Journal: Quantitative imaging in medicine and surgery

Published: September 29, 2025

DLL1 haploinsufficiency in prenatal brain anomalies: a retrospective analysis of 6q terminal deletions.

DLL1 haploinsufficiency in prenatal brain anomalies: a retrospective analysis of 6q terminal deletions.

Journal: Frontiers in genetics

Published: June 04, 2025

Fetal umbilical-portal-systemic venous shunt diagnosed by prenatal ultrasonography and its association with chromosomal abnormalities.

Fetal umbilical-portal-systemic venous shunt diagnosed by prenatal ultrasonography and its association with chromosomal abnormalities.

Journal: Quantitative imaging in medicine and surgery

Published: February 25, 2025

Maternal and fetal risk factors for congenital anomalies of the kidney and urinary tract: a birth cohort study in urban China.

Maternal and fetal risk factors for congenital anomalies of the kidney and urinary tract: a birth cohort study in urban China.

Journal: Journal of nephrology

Published: February 01, 2024

Mutation spectrum of hearing loss patients in Northwest China: Identification of 20 novel variants.

Mutation spectrum of hearing loss patients in Northwest China: Identification of 20 novel variants.

Journal: Molecular genetics & genomic medicine

Published: November 15, 2023

Prenatal Ultrasound Diagnosis of Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome with Persistent Hyperplastic Primary Vitreous: A Case Report.

Prenatal Ultrasound Diagnosis of Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome with Persistent Hyperplastic Primary Vitreous: A Case Report.

Journal: Fetal diagnosis and therapy

Published: June 27, 2023

Genetic analysis and literature review of a Poirier-Bienvenu neurodevelopmental syndrome family line caused by a de novo frameshift variant in CSNK2B.

Genetic analysis and literature review of a Poirier-Bienvenu neurodevelopmental syndrome family line caused by a de novo frameshift variant in CSNK2B.

Journal: Molecular genetics & genomic medicine

Published: May 15, 2023

Immune skeletal dysplasia with neurodevelopmental abnormalities caused by a novel variant of EXTL3 gene in a Chinese family.

Immune skeletal dysplasia with neurodevelopmental abnormalities caused by a novel variant of EXTL3 gene in a Chinese family.

Journal: Molecular genetics & genomic medicine

Published: April 13, 2023

ATP9A knockdown leads to neurite fracture and retraction.

ATP9A knockdown leads to neurite fracture and retraction.

Journal: Molecular psychiatry

Published: March 10, 2023

Three Variants Affecting Exon 1 of Ectodysplasin A Cause X-Linked Hypohidrotic Ectodermal Dysplasia: Clinical and Molecular Characteristics.

Three Variants Affecting Exon 1 of Ectodysplasin A Cause X-Linked Hypohidrotic Ectodermal Dysplasia: Clinical and Molecular Characteristics.

Journal: Frontiers in genetics

Published: April 09, 2022

Maternal fish and shellfish consumption and preterm birth: a retrospective study in urban China.

Maternal fish and shellfish consumption and preterm birth: a retrospective study in urban China.

Journal: The British journal of nutrition

Published: September 24, 2021

Showing 1-12 of 15

Last Updated: 09/26/2026