Genetic Laboratory

The Genetic Laboratory is one of the hospital's key diagnostic platforms, dedicated to providing genetic-level technical support for clinical diagnosis and treatment.

The laboratory is constructed and managed in strict compliance with national standards and regulations, equipped with professional technicians and advanced instruments to ensure the accuracy and reliability of test results.

The laboratory currently offers the following testing services:

• Chromosome Karyotype Analysis

  Detects chromosomal numerical and structural abnormalities, such as Down syndrome and Turner syndrome.

• Genomic Copy Number Variation (CNV) Detection

  Utilizes next-generation sequencing (NGS) technology to detect chromosomal microdeletions and microduplications.

• Whole Exome Sequencing (WES)

  Employs sequence capture technology to enrich and analyze exome regions via high-throughput sequencing, identifying variants and discovering novel genes.

• Fluorescence In Situ Hybridization (FISH)

  Enables rapid detection of common chromosomal numerical abnormalities, effectively compensating for the long turnaround time of karyotype analysis.

The Genetic Laboratory adheres to a patient-centered approach, upholding rigorous and scientific standards to deliver high-quality testing services.

Note: The above content is for reference only. Specific testing services are subject to the hospital's actual offerings.