PGT-M/PGT-SR_Unimed Biotech(Shanghai)Co.，Ltd

Clinic Lab

Introduction
Expert team
Certificates

Platforms

Single cell capture platform
Microarray platform
NGS platform

Tests

PGT-M/PGT-SR
PGT-A
Prenatal genetic diagnosis
cb-NIPT
Noninvasive prenatal paternity test
Neonatal genetic disease screening
Genetic analysis of misarriages
Genetic screening
Fragile X syndrome screening
AZF microdeletion and sex chromosome aneuploidy screening
Clinical whole exome sequencing
CNV-seq

Research

Endometrial receptivity assessment
Circulating tumor cell capture

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Clinic test

Home Clinical detection PGT-M/PGT-SR Testing Content

PGT-M/PGT-SR

Column List

PGT-M/PGT-SR
PGT-A
Prenatal genetic diagnosis
cb-NIPT
Noninvasive prenatal paternity test
Neonatal genetic disease screening
Genetic analysis of misarriages
Genetic screening
Fragile X syndrome screening
AZF microdeletion and sex chromosome aneuploidy screening
Clinical whole exome sequencing
CNV-seq

• Balanced translocation of chromosomes
• Robertsonian translocation
• Single genetic disease
• HLA matching
• Hereditary tumor

Unit 905,TOWER 1,LANDMRK,CENTER,NO.328 Tiantong Rd,Shanghai

4008-213-671

infor@unimeddx.com

www.unimeddx.com

Introduction
Expert team
Certificates

Single cell capture platform
Microarray platform
NGS platform

PGT-M/PGT-SR
PGT-A
Prenatal genetic diagnosis
cb-NIPT
Noninvasive prenatal paternity test
Neonatal genetic disease screening
Genetic analysis of misarriages
Genetic screening
Fragile X syndrome screening
AZF microdeletion and sex chromosome aneuploidy screening
Clinical whole exome sequencing
CNV-seq

Endometrial receptivity assessment
Circulating tumor cell capture

Company news
Marketing activities
Science news
Documents

About Unimed
Managemet team
Partners
Recruitment
Contact us

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