Linjie Pu
Tianjin, China
Last Updated: 09/26/2026
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Found 9 publications
Single nucleotide polymorphisms of PCP pathway related genes participate in the occurrence and development of neural tube defect.
Journal: Molecular genetics & genomic medicine
Published: July 18, 2022
Vitamin D levels and Vitamin D-related gene polymorphisms in Chinese children with type 1 diabetes.
Journal: Frontiers in pediatrics
Published: June 09, 2022
Identification of two aberrant transcripts by RNA sequencing for a novel variant c.3354 + 5 G > A of MED12 in a Chinese girl with non-syndromic intellectual disability.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: March 18, 2022
Efficacy and Safety of Diet Therapies in Children With Autism Spectrum Disorder: A Systematic Literature Review and Meta-Analysis.
Journal: Frontiers in neurology
Published: December 27, 2021
A functional study for verifying the pathogenicity of a TRPM6 variant of uncertain significance: A novel non-canonical splicing-site variant in primary hypomagnesemia with secondary hypocalcemia.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: October 08, 2021
Clinical study of autoantibodies in type 1 diabetes mellitus children with ketoacidosis or microalbuminuria.
Journal: Journal of clinical laboratory analysis
Published: October 07, 2021
A cohort of five cases with asymmetric conjoined twining and literature review.
Journal: Pediatric surgery international
Published: August 26, 2021
What is the impact of a novel DEPDC5 variant on an infant with focal epilepsy: a case report.
Journal: BMC pediatrics
Published: May 10, 2021
High-throughput screening reveals novel mutations in spinal muscular atrophy patients.
Journal: Italian journal of pediatrics
Published: April 06, 2020
Showing 1-9 of 9
Last Updated: 09/26/2026