Bao-sheng Zhu

NHC Key Laboratory Of Healthy Birth And Birth Defect Prevention In Western China, Key Laboratory Of Birth Defect And Genetic Disease Research Of Yunnan Province
Kunming, 650032, China

Last Updated: 09/26/2026

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Found 16 publications

Expert consensus on the morphological characteristics diagnostic criteria and genetic counseling of human chromosomal polymorphisms.

Expert consensus on the morphological characteristics diagnostic criteria and genetic counseling of human chromosomal polymorphisms.

Journal: Yi chuan = Hereditas

Published: January 18, 2026

Combined biochemical and genetic analysis improves early diagnosis and prenatal assessment of multiple acyl-CoA dehydrogenase deficiency.

Combined biochemical and genetic analysis improves early diagnosis and prenatal assessment of multiple acyl-CoA dehydrogenase deficiency.

Journal: World journal of pediatrics : WJP

Published: November 05, 2025

Expert consensus on the combined screening of genes and biomarkers for neonatal diseases.

Expert consensus on the combined screening of genes and biomarkers for neonatal diseases.

Journal: World journal of pediatrics : WJP

Published: July 07, 2025

Genetic screening and follow-up results in 3 001 newborns in the Yunnan region

Genetic screening and follow-up results in 3 001 newborns in the Yunnan region

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics

Published: June 30, 2025

Ginsenoside Rg1 promotes fetal hemoglobin production in vitro: A potential therapeutic avenue for β-thalassemia.

Ginsenoside Rg1 promotes fetal hemoglobin production in vitro: A potential therapeutic avenue for β-thalassemia.

Journal: European journal of pharmacology

Published: November 10, 2023

Identification of a Novel 7-bp Deletion in the α-Globin Gene Cluster in One Chinese Family.

Identification of a Novel 7-bp Deletion in the α-Globin Gene Cluster in One Chinese Family.

Journal: Hemoglobin

Published: May 29, 2023

Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China.

Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China.

Journal: BMC medical genomics

Published: February 10, 2023

Association of copy number of SMN1 and SMN2 with clinical phenotypes in children with spinal muscular atrophy

Association of copy number of SMN1 and SMN2 with clinical phenotypes in children with spinal muscular atrophy

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics

Published: March 26, 2019

Novel DOCK7 mutations in a Chinese patient with early infantile epileptic encephalopathy 23.

Novel DOCK7 mutations in a Chinese patient with early infantile epileptic encephalopathy 23.

Journal: Chinese medical journal

Published: February 27, 2019

Ethical considerations for conducting sexual and reproductive health research with female adolescents engaged in high-risk behaviours in China.

Ethical considerations for conducting sexual and reproductive health research with female adolescents engaged in high-risk behaviours in China.

Journal: Sexual & reproductive healthcare : official journal of the Swedish Association of Midwives

Published: March 20, 2018

Analysis of treatment efficacy for congenital hypothyroidism in some regions of Yunnan Province, China

Analysis of treatment efficacy for congenital hypothyroidism in some regions of Yunnan Province, China

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics

Published: July 13, 2017

Genetic heterogeneity of the β-globin gene in various geographic populations of Yunnan in southwestern China.

Genetic heterogeneity of the β-globin gene in various geographic populations of Yunnan in southwestern China.

Journal: PloS one

Published: October 04, 2014

Showing 1-12 of 16

Last Updated: 09/26/2026