An Liu
123 Tianfei Alley
Nanjing, 210004, China
Nanjing, 210004, China
Last Updated: 09/26/2026
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Found 9 publications
Long read Nanopore sequencing identifies precise breakpoints of a de novo paracentric inversion that disrupt the MEIS2 gene in a Chinese girl with syndromic developmental delay.
Journal: BMC pediatrics
Published: August 23, 2024
Optical Genome Mapping for Chromosomal Aberrations Detection-False-Negative Results and Contributing Factors.
Journal: Diagnostics (Basel, Switzerland)
Published: December 06, 2023
Optical genome mapping for detection of chromosomal aberrations in prenatal diagnosis.
Journal: Acta obstetricia et gynecologica Scandinavica
Published: March 28, 2023
11q13.3q13.4 deletion plus 9q21.13q21.33 duplication in an affected girl arising from a familial four-way balanced chromosomal translocation.
Journal: Molecular genetics & genomic medicine
Published: January 17, 2023
A capillary electrophoresis-based variant hotspot genotyping method for rapid and reliable analysis of the phenylalanine hydroxylase gene in the Chinese Han population.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: August 24, 2021
Diagnosis of Shashi-Pena Syndrome Caused by Chromosomal Rearrangement Using Nanopore Sequencing.
Journal: Neurology. Genetics
Published: April 26, 2021
Analyzing false-negative results detected in low-risk non-invasive prenatal screening cases.
Journal: Molecular genetics & genomic medicine
Published: May 23, 2019
Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies.
Journal: Frontiers in genetics
Published: April 20, 2018
Perinatal outcomes following cell-free DNA screening in >32 000 women: Clinical follow-up data from a single tertiary center.
Journal: Prenatal diagnosis
Published: March 14, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026