Chiyan Zhou

East Zhong Huan Road, 2468#
Jiaxing, 314050, China

Last Updated: 09/26/2026

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Found 13 publications

Genetic Analysis of a Patient with β-Thalassemia Major and Homozygous Hb Constant Spring in a Chinese Family.

Genetic Analysis of a Patient with β-Thalassemia Major and Homozygous Hb Constant Spring in a Chinese Family.

Journal: Clinical laboratory
Published: November 12, 2025

A nomogram to predict pulmonary complications after gastrointestinal surgery: a retrospective study.

A nomogram to predict pulmonary complications after gastrointestinal surgery: a retrospective study.

Journal: BMC gastroenterology
Published: July 27, 2024

Compound heterozygous variants in SLC45A1 might cause syndromic intellectual disability by localization failure and activity attenuation in cells.

Compound heterozygous variants in SLC45A1 might cause syndromic intellectual disability by localization failure and activity attenuation in cells.

Journal: Clinical genetics
Published: April 04, 2024

Carrier screening and prenatal diagnosis for thalassemia-associated mutations in Jiaxing area of Zhejiang

Carrier screening and prenatal diagnosis for thalassemia-associated mutations in Jiaxing area of Zhejiang

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 28, 2023

Incidence and genetic reproductive characteristics of AZFc microdeletion among patients with azoospermia or severe oligospermia

Incidence and genetic reproductive characteristics of AZFc microdeletion among patients with azoospermia or severe oligospermia

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 30, 2022

Dynamic metabolic profiles for HBeAg seroconversion in chronic hepatitis B (CHB) patients by gas chromatography-mass spectrometry (GC-MS).

Dynamic metabolic profiles for HBeAg seroconversion in chronic hepatitis B (CHB) patients by gas chromatography-mass spectrometry (GC-MS).

Journal: Journal of pharmaceutical and biomedical analysis
Published: March 11, 2021

A Beckwith-Wiedemann syndrome case with de novo 24 Mb duplication of chromosome 11p15.5p14.3.

A Beckwith-Wiedemann syndrome case with de novo 24 Mb duplication of chromosome 11p15.5p14.3.

Journal: Molecular cytogenetics
Published: November 14, 2020

Application of non-invasive prenatal testing for the screening of fetal chromosomal abnormalities in 12 085 cases

Application of non-invasive prenatal testing for the screening of fetal chromosomal abnormalities in 12 085 cases

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 14, 2020

Prenatal diagnosis of rearrangements in the fetal 22q11.2 region.

Prenatal diagnosis of rearrangements in the fetal 22q11.2 region.

Journal: Molecular cytogenetics
Published: February 11, 2020

Prenatal diagnosis of a novel SOX10 mutation in a patient with syndromic hearing loss

Prenatal diagnosis of a novel SOX10 mutation in a patient with syndromic hearing loss

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 29, 2019

Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene

Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 01, 2019

A case of Wolf-Hirschhorn syndrome diagnosed by single nucleotide polymorphism array

A case of Wolf-Hirschhorn syndrome diagnosed by single nucleotide polymorphism array

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 26, 2016
Showing 1-12 of 13

Last Updated: 09/26/2026