Nan Liu
Tianjin, 300134, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Association of IRX6 rs6499755 and HAAO rs3816183 Polymorphisms With Hypospadias Susceptibility in Northern Chinese Han Population.
Journal: Genetics research
Published: September 27, 2024
Refining the genetic diagnostic puzzle: A case report on a Chinese ARPKD patient with a reciprocal balanced translocation and c.2507 T > C (p.V836A) in PKHD1.
Journal: Nephrology (Carlton, Vic.)
Published: April 15, 2024
Advances in the Structures, Pharmacological Activities, and Biosynthesis of Plant Diterpenoids.
Journal: Journal of microbiology and biotechnology
Published: February 08, 2024
Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report.
Journal: Italian journal of pediatrics
Published: March 21, 2023
Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report.
Journal: Italian journal of pediatrics
Published: September 01, 2022
Genetic analysis of 46,XY disorders of sex development in children caused by a new NR5A1 gene variant
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 03, 2021
The spectrum of CYP21A2 gene mutations in patients with classic salt wasting form of 2l-hydroxylase deficiency in a Chinese cohort.
Journal: Molecular genetics & genomic medicine
Published: May 18, 2020
Origin and morphological features of small supernumerary marker chromosomes in Turner syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 09, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026