Libin Mei

Fujian Key Clinical Specialty Of Laboratory Medicine
Xiamen, China

Last Updated: 09/26/2026

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Found 39 publications

Genetic analysis of F8 mutations in five hemophilia a carriers.

Genetic analysis of F8 mutations in five hemophilia a carriers.

Journal: Frontiers in medicine

Published: February 06, 2026

Characterization of a Splice Variant in FLNA Associated With Periventricular Nodular Heterotopia.

Characterization of a Splice Variant in FLNA Associated With Periventricular Nodular Heterotopia.

Journal: Neurology. Genetics

Published: June 02, 2025

Preimplantation Genetic Testing in a Family with Neurofibromatosis Type 1.

Preimplantation Genetic Testing in a Family with Neurofibromatosis Type 1.

Journal: Genetic testing and molecular biomarkers

Published: February 14, 2025

Splice‑site variant c.3531+1G>T in COL1A1 in a family with osteogenesis imperfecta.

Splice‑site variant c.3531+1G>T in COL1A1 in a family with osteogenesis imperfecta.

Journal: Molecular medicine reports

Published: November 05, 2024

Preimplantation Genetic Testing Inhibits the Transmission of Pathogenic Variants Associated With Cerebral White Matter Disease.

Preimplantation Genetic Testing Inhibits the Transmission of Pathogenic Variants Associated With Cerebral White Matter Disease.

Journal: Cureus

Published: July 23, 2024

Preimplantation genetic testing for Cockayne syndrome with a novel ERCC6 variant in a Chinese family.

Preimplantation genetic testing for Cockayne syndrome with a novel ERCC6 variant in a Chinese family.

Journal: Frontiers in genetics

Published: May 20, 2024

Day 2 versus day 3 embryo transfer in patients with in vitro fertilization and only one zygote with two pronuclei.

Day 2 versus day 3 embryo transfer in patients with in vitro fertilization and only one zygote with two pronuclei.

Journal: The Journal of international medical research

Published: March 28, 2024

Corrigendum: Mutations in FIGLA associated with premature ovarian insufficiency in a Chinese population.

Corrigendum: Mutations in FIGLA associated with premature ovarian insufficiency in a Chinese population.

Journal: Frontiers in medicine

Published: May 17, 2022

Genetic analysis of a Chinese pedigree affected with congenital split-hand/foot malformation

Genetic analysis of a Chinese pedigree affected with congenital split-hand/foot malformation

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: November 28, 2021

Clinical and molecular genetic analysis of a patient with 3-M syndrome

Clinical and molecular genetic analysis of a patient with 3-M syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: November 28, 2021

Two novel biallelic mutations in PSMC3IP in a patient affected by premature ovarian insufficiency.

Two novel biallelic mutations in PSMC3IP in a patient affected by premature ovarian insufficiency.

Journal: Molecular medicine reports

Published: August 16, 2021

Mutations in FIGLA Associated With Premature Ovarian Insufficiency in a Chinese Population.

Mutations in FIGLA Associated With Premature Ovarian Insufficiency in a Chinese Population.

Journal: Frontiers in medicine

Published: May 25, 2021

Showing 1-12 of 39

Last Updated: 09/26/2026