Xiang-dong Kong

Zhengzhou, 450052, China

Last Updated: 09/26/2026

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Found 14 publications

The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.

The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.

Journal: Innovation (Cambridge (Mass.))
Published: July 11, 2024

Mutations in the γ-secretase genes PSEN1, PSENEN, and NCSTN in a family with acne inversa.

Mutations in the γ-secretase genes PSEN1, PSENEN, and NCSTN in a family with acne inversa.

Journal: European journal of dermatology : EJD
Published: August 15, 2018

Neonatal lethality and recycling defect of transferrin receptor in mice with Syntaxin12/13 disruption.

Neonatal lethality and recycling defect of transferrin receptor in mice with Syntaxin12/13 disruption.

Journal: Protein & cell
Published: March 08, 2018

The association between an endothelial nitric oxide synthase gene polymorphism and coronary heart disease in young people and the underlying mechanism.

The association between an endothelial nitric oxide synthase gene polymorphism and coronary heart disease in young people and the underlying mechanism.

Journal: Molecular medicine reports
Published: May 12, 2017

High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencing.

High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencing.

Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: April 20, 2017

Nerve growth factor for the treatment of spinocerebellar ataxia type 3: an open-label study.

Nerve growth factor for the treatment of spinocerebellar ataxia type 3: an open-label study.

Journal: Chinese medical journal
Published: January 31, 2015

A novel 1-bp deletion mutation of the EDA gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia.

A novel 1-bp deletion mutation of the EDA gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia.

Journal: The Journal of dermatology
Published: July 03, 2014

Screening of human chromosome 21 genes in the dorsolateral prefrontal cortex of individuals with Down syndrome.

Screening of human chromosome 21 genes in the dorsolateral prefrontal cortex of individuals with Down syndrome.

Journal: Molecular medicine reports
Published: February 13, 2014

Mutation analysis and first-trimester prenatal diagnosis for a Chinese family with hidrotic ectodermal dysplasia

Mutation analysis and first-trimester prenatal diagnosis for a Chinese family with hidrotic ectodermal dysplasia

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 09, 2013

Mutation analysis and prenatal diagnosis of a Chinese family with X-linked severe combined immunodeficiency

Mutation analysis and prenatal diagnosis of a Chinese family with X-linked severe combined immunodeficiency

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: January 11, 2013

Karyotype analysis in large-sample infertile couples living in Central China: a study of 14965 couples.

Karyotype analysis in large-sample infertile couples living in Central China: a study of 14965 couples.

Journal: Journal of assisted reproduction and genetics
Published: October 30, 2012

Early prenatal genetic diagnosis of oculocutaneous albinism type I in seven families

Early prenatal genetic diagnosis of oculocutaneous albinism type I in seven families

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 10, 2012
Showing 1-12 of 14

Last Updated: 09/26/2026