Shu Liu
Guangzhou, 511442, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
Association Between Socioeconomic Indicators and Growth Hormone Treatment Patterns for Idiopathic Short Stature in China: A Large-Scale Real-World Study.
Journal: Advances in therapy
Published: February 11, 2026
Potential role of ARG1 c.57G > A variant in Argininemia.
Journal: Genes & genomics
Published: June 20, 2024
Two Chinese Patients of Auriculocondylar Syndrome 2: A Novel PLCB4 Splicing Variant and 5-Year Follow-up.
Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: February 28, 2024
Delayed Biotin Therapy in a Child with Atypical Profound Biotinidase Deficiency: Late Arrival of the Truth and a Lesson Worth Thinking.
Journal: International journal of molecular sciences
Published: May 10, 2023
Case Report: Successful Management of a 29-Day-Old Infant With Severe Hyperlipidemia From a Novel Homozygous Variant of GPIHBP1 Gene.
Journal: Frontiers in pediatrics
Published: October 10, 2021
Transmission of a Novel Imprinting Center Deletion Associated With Prader-Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About.
Journal: Frontiers in genetics
Published: December 03, 2020
Genetic testing for Prader-Willi syndrome and Angelman syndrome in the clinical practice of Guangdong Province, China.
Journal: Molecular cytogenetics
Published: December 16, 2018
Possibility of early diagnosis in a fetus affected by Prader‑Willi syndrome with maternal hetero‑UPD15: A lesson to be learned.
Journal: Molecular medicine reports
Published: October 15, 2018
Prenatal diagnosis in a hereditary Peutz-Jeghers syndrome family with high cancer risk.
Journal: BMC medical genetics
Published: September 12, 2017
Uniparental Disomy of Chromosome 15 in Two Cases by Chromosome Microarray: A Lesson Worth Thinking.
Journal: Cytogenetic and genome research
Published: April 12, 2017
Two novel mutations in the glycine decarboxylase gene in a boy with classic nonketotic hyperglycinemia: case report.
Journal: Archivos argentinos de pediatria
Published: October 19, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026