Kai Jiang

Changchun, China

Last Updated: 09/26/2026

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Found 22 publications

Efficacy of long-acting growth hormone in Axenfeld-Rieger syndrome with a novel 3.824 Mb 4q25 deletion: a Case Report and systematic literature review.

Efficacy of long-acting growth hormone in Axenfeld-Rieger syndrome with a novel 3.824 Mb 4q25 deletion: a Case Report and systematic literature review.

Journal: Frontiers in genetics

Published: April 15, 2026

A case report of X-linked ichthyosis associated with epilepsy due to an Xp22.31 deletion fragment.

A case report of X-linked ichthyosis associated with epilepsy due to an Xp22.31 deletion fragment.

Journal: Frontiers in medicine

Published: November 06, 2025

Navigating the complexities of dual CNV findings: a case of DEE7 caused by a de novo KCNQ2 deletion and a Co-occurring chromosome 13 duplication - a case report and literature review.

Navigating the complexities of dual CNV findings: a case of DEE7 caused by a de novo KCNQ2 deletion and a Co-occurring chromosome 13 duplication - a case report and literature review.

Journal: Frontiers in pediatrics

Published: November 02, 2025

Coral-Inspired Biomimetic Hydrophilic Nano-PEEK Surface Reinforced by Fluorescence for Effective Antifouling Performance.

Coral-Inspired Biomimetic Hydrophilic Nano-PEEK Surface Reinforced by Fluorescence for Effective Antifouling Performance.

Journal: Nano letters

Published: September 28, 2025

Cartilage-hair hypoplasia in a patient with compound heterozygous variants in the RMRP gene: A case report.

Cartilage-hair hypoplasia in a patient with compound heterozygous variants in the RMRP gene: A case report.

Journal: Medicine

Published: August 24, 2025

Concurrent 12p trisomy and 4q34.2-q35.2 deletion detected by WES-CNV: Case report.

Concurrent 12p trisomy and 4q34.2-q35.2 deletion detected by WES-CNV: Case report.

Journal: Medicine

Published: August 19, 2025

A case of childhood hyperekplexia due to a novel nonsense variant in the GLRA1 gene.

A case of childhood hyperekplexia due to a novel nonsense variant in the GLRA1 gene.

Journal: Medicine

Published: August 06, 2025

De novo missense mutation in MYT1l leading to autosomal dominant intellectual disability 39 and autism spectrum disorder: a case report.

De novo missense mutation in MYT1l leading to autosomal dominant intellectual disability 39 and autism spectrum disorder: a case report.

Journal: Frontiers in pediatrics

Published: July 25, 2025

De novo frameshift mutation in SYNGAP1 resulting in autosomal dominant mental retardation type 5 and autism spectrum disorder: a case report.

De novo frameshift mutation in SYNGAP1 resulting in autosomal dominant mental retardation type 5 and autism spectrum disorder: a case report.

Journal: Frontiers in pediatrics

Published: July 23, 2025

Confined Dynamic and Static Disorder Realized by Entropy Engineering, a New Path to Excellent High Temperature Energy Storage Performance.

Confined Dynamic and Static Disorder Realized by Entropy Engineering, a New Path to Excellent High Temperature Energy Storage Performance.

Journal: Advanced materials (Deerfield Beach, Fla.)

Published: June 17, 2025

A colorimetric/fluorescent dual-mode aptasensor for the rapid and sensitive detection of Listeria monocytogenes.

A colorimetric/fluorescent dual-mode aptasensor for the rapid and sensitive detection of Listeria monocytogenes.

Journal: iScience

Published: April 17, 2025

Phelan-McDermid syndrome in a Chinese pediatric patient: A case report - new heterozygous mutations lead to PMS.

Phelan-McDermid syndrome in a Chinese pediatric patient: A case report - new heterozygous mutations lead to PMS.

Journal: Medicine

Published: February 18, 2025

Showing 1-12 of 22

Last Updated: 09/26/2026