Ti-zhen Yan

Liuzhou, 545001, China

Last Updated: 09/26/2026

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Found 14 publications

Molecular Diagnosis and Pedigree Analysis of Rare Mutations in Non-coding Region of HBA2 Gene

Molecular Diagnosis and Pedigree Analysis of Rare Mutations in Non-coding Region of HBA2 Gene

Journal: Zhongguo shi yan xue ye xue za zhi

Published: June 27, 2024

Cases Analysis of Hemoglobin H Disease Caused by HBA2:c.2T>C and HBA2:c.2delT Mutations

Cases Analysis of Hemoglobin H Disease Caused by HBA2:c.2T>C and HBA2:c.2delT Mutations

Journal: Zhongguo shi yan xue ye xue za zhi

Published: April 25, 2024

Methodological Evaluation of Microarray in the Detection of α-Thalassemia

Methodological Evaluation of Microarray in the Detection of α-Thalassemia

Journal: Zhongguo shi yan xue ye xue za zhi

Published: December 11, 2021

Application of DNA Microarray in Genetic Mutation Detection in Patients with Thalassemia

Application of DNA Microarray in Genetic Mutation Detection in Patients with Thalassemia

Journal: Zhongguo shi yan xue ye xue za zhi

Published: October 10, 2021

Pedigree Analysis of Nonhomologous Sequence Recombination of HBA1 and HBA2 Genes.

Pedigree Analysis of Nonhomologous Sequence Recombination of HBA1 and HBA2 Genes.

Journal: Hemoglobin

Published: August 20, 2020

Clinical and cytogenetic study in a child with de novo chromosome 9 abnormality

Clinical and cytogenetic study in a child with de novo chromosome 9 abnormality

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

Published: January 17, 2018

Genetic diagnosis of 10 neonates with primary carnitine deficiency

Genetic diagnosis of 10 neonates with primary carnitine deficiency

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

Published: November 15, 2017

CPT2 gene mutation analysis and prenatal diagnosis in a family with carnitine palmitoyltransferase II deficiency

CPT2 gene mutation analysis and prenatal diagnosis in a family with carnitine palmitoyltransferase II deficiency

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

Published: December 16, 2016

Pancytopenia and metabolic decompensation in a neonate

Pancytopenia and metabolic decompensation in a neonate

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

Published: November 08, 2016

Identification of gene mutation and prenatal diagnosis in a family with X-linked ichthyosis

Identification of gene mutation and prenatal diagnosis in a family with X-linked ichthyosis

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

Published: November 08, 2016

An analysis of clinical characteristics and gene mutation in two patients with medium- and short-chain acyl-CoA dehydrogenase deficiency

An analysis of clinical characteristics and gene mutation in two patients with medium- and short-chain acyl-CoA dehydrogenase deficiency

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

Published: October 19, 2016

Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy.

Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy.

Journal: Clinical chemistry and laboratory medicine

Published: April 05, 2016

Showing 1-12 of 14

Last Updated: 09/26/2026