Qi Luo
Quanzhou, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report.
Journal: Frontiers in genetics
Published: June 08, 2022
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature review.
Journal: Molecular genetics & genomic medicine
Published: February 23, 2022
A First Clinical and Molecular Study of Rare IVS-II-806 (G > C) (HBB:c.316-45G > C) Variant in the β-globin Gene: A Possibly Benign Variant.
Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
Published: December 11, 2021
Identification of a Rare Variant of c.1777G>A (p.G593S) in the COL1A1 Gene as the Etiology of Recurrent Osteogenesis Imperfecta by Whole-Exome Sequencing.
Journal: Frontiers in pediatrics
Published: November 16, 2021
Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese population.
Journal: Molecular cytogenetics
Published: October 13, 2021
The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis.
Journal: Frontiers in pediatrics
Published: July 19, 2021
Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, China.
Journal: BMC pregnancy and childbirth
Published: November 02, 2020
Simvastatin inhibits inflammation in ischemia-reperfusion injury.
Journal: Inflammation
Published: June 11, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026