Zemin Luo
Chengdu, China
Last Updated: 09/26/2026
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Found 11 publications
A novel NSD2 pathogenic variant in a Chinese patient with Rauch-Steindl syndrome: a case report.
Journal: BMC neurology
Published: September 13, 2025
CUX1 variant and 9p deletion: expanding the spectrum and resolving variable GDD/ID in a family.
Journal: BMC medical genomics
Published: May 31, 2025
Genetic analysis of partial duplication of the long arm of chromosome 16.
Journal: BMC medical genomics
Published: September 10, 2024
Genotype-phenotype correlation of ODLURO syndrome comorbid epilepsy associated with KMT2E variations: Report on a novel case and systematic literature review.
Journal: Epilepsy & behavior : E&B
Published: August 11, 2024
Nephrogenic diabetes insipidus results from a novel in-frame deletion of AVPR2 gene in monozygotic-twin boys and their mother and grandmother.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: July 01, 2024
Dual diagnosis of microcephalic osteosplastic primary dwarfism type II and benign familial infantile seizure type 2: a case report.
Journal: Clinical dysmorphology
Published: March 05, 2024
Acute Necrotizing Encephalopathy Associated with SARS-CoV-2 Infection in Children.
Journal: Annals of Indian Academy of Neurology
Published: October 14, 2023
Genotype characterization of tetrahydrobiopterin deficiency in two Tibetan children.
Journal: Heliyon
Published: June 03, 2023
Genetic analysis of a pedigree with MECP2 duplication syndrome in China.
Journal: BMC medical genomics
Published: February 25, 2023
Showing 1-11 of 11
Last Updated: 09/26/2026