Qinle Zhang
Nanning, China
Last Updated: 09/26/2026
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Found 23 publications
Frameshift variants in the UBTF gene are associated with neurodevelopmental disorders.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: October 28, 2025
Novel variants in STAG2 and PKD1 associate with multiple congenital malformations and autosomal dominant polycystic kidney disease in a Chinese family: A case report and literature review.
Journal: Experimental and therapeutic medicine
Published: June 06, 2025
Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience.
Journal: Orphanet journal of rare diseases
Published: May 20, 2025
Clinical and Genetic Analysis of SMARCC2-Related Diseases in Three Chinese Patients.
Journal: Molecular genetics & genomic medicine
Published: April 30, 2025
Novel Compound Heterozygous Variants in the TCTN2 Gene Causing Meckel-Gruber Syndrome 8 in a Non-Consanguineous Chinese Family.
Journal: Molecular genetics & genomic medicine
Published: October 10, 2024
Rational designed Fe-ZIFs@CoP nanoplatforms for photothermal-enhanced ROS-mediated tumor therapy.
Journal: Frontiers in bioengineering and biotechnology
Published: December 25, 2023
Upregulation of CALD1 predicted a poor prognosis for platinum-treated ovarian cancer and revealed it as a potential therapeutic resistance target.
Journal: BMC genomics
Published: August 08, 2023
Novel compound heterozygous variants in the RPL3L gene causing dilated cardiomyopathy type-2D: a case report and literature review.
Journal: BMC medical genomics
Published: March 18, 2023
Last Updated: 09/26/2026