Yu Tan
Chengdu, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 31 publications
A Case of Monozygotic Twins Carrying a Novel Loss-of-Function Variant in the MYCBP2 Gene, Presenting With Microcephaly, Ectopic Kidney and Growth Restriction.
Journal: Prenatal diagnosis
Published: January 30, 2026
Correction: De Novo CHD7 variant in a CHARGE syndrome preterm infant initially diagnosed as idiopathic hypogonadotropic hypogonadism: a case report and literature review.
Journal: BMC pediatrics
Published: December 30, 2025
De novo CHD7 variant in a CHARGE syndrome preterm infant initially diagnosed as idiopathic hypogonadotropic hypogonadism: a case report and literature review.
Journal: BMC pediatrics
Published: April 13, 2025
Application of HIrisPlex-S System in Forensic DNA Phenotyping
Journal: Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition
Published: April 02, 2025
Corrigendum: Set of 15 SNP-SNP markers for detection of unbalanced degraded DNA mixtures and noninvasive prenatal paternity testing.
Journal: Frontiers in genetics
Published: January 06, 2025
Measures and effects on soil Cd remediation and safe rice production: a meta-analysis of 10-year Chinese patents.
Journal: International journal of phytoremediation
Published: December 05, 2024
Limitations of homologous recombination status testing and poly (ADP-ribose) polymerase inhibitor treatment in the current management of ovarian cancer.
Journal: Frontiers in oncology
Published: May 19, 2024
Screening a new set of microhaplotypes in exonic regions for sample identity testing and paternity testing during whole exome sequencing analysis.
Journal: International journal of legal medicine
Published: March 26, 2024
A case of congenital cataracts with hypotrichosis caused by compound heterozygous variants in the LSS gene.
Journal: Molecular genetics & genomic medicine
Published: June 16, 2023
A dual-channel secondary closed-loop supply chain considering retail groups and fairness concerns.
Journal: PloS one
Published: May 05, 2023
A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney disease.
Journal: Molecular genetics & genomic medicine
Published: April 03, 2023
Applying amplification refractory mutation system technique to detecting cell-free fetal DNA for single-gene disorders purpose.
Journal: Frontiers in genetics
Published: October 16, 2022
Last Updated: 09/26/2026