Showing 161–176 of 253 results

- - Blood Spot
  - Genetic Disorders
  - Immunoassay
  - Lab Test
  - Newborns
  - PCR
  - Varies by condition
  (0)
  
  Newborn screening test panel
  
  ฿32,292.00
  
  Screens newborns for various metabolic and genetic disorders like galactosemia, cystic fibrosis, and adrenal hyperplasia.
  
  Add to cart
- Add to cart
  - Blood Spot
  Newborn screening test panel
  (0)
  ฿32,292.00
- - Adults
  - Chromosomal Abnormalities
  - Genetic Disorders
  - Lab Test
  - Massively Parallel Sequencing
  - N/A
  - None
  - Prenatal
  - Whole Blood
  (0)
  
  NIFTY Test [BGI]
  
  ฿35,200.00
  
  A non-invasive prenatal screening test that detects fetal chromosomal abnormalities such as Down syndrome, Edwards syndrome, and Patau syndrome using…
  
  Add to cart
- Add to cart
  - Adults
  NIFTY Test [BGI]
  (0)
  ฿35,200.00
- - All Ages
  - Blood
  - Difficulty Swallowing
  - Drooping Eyelids
  - Family History
  - Genetic Disorders
  - Lab Test
  - PCR + DNA Sequencing
  (0)
  
  Oculopharyngeal muscular dystrophy
  
  ฿7,770.00
  
  Detects mutations associated with oculopharyngeal muscular dystrophy.
  
  Add to cart
- Add to cart
  - All Ages
  Oculopharyngeal muscular dystrophy
  (0)
  ฿7,770.00
- - All Ages
  - Blood
  - Fatigue
  - Genetic Disorders
  - Jaundice
  - Lab Test
  - None
  - Osmotic Fragility Test
  (0)
  
  OF test for hereditary spherocytosis
  
  ฿840.00
  
  Detects hereditary spherocytosis, a genetic disorder causing abnormal red blood cells.
  
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- Add to cart
  - All Ages
  OF test for hereditary spherocytosis
  (0)
  ฿840.00
- - Adults
  - Anemia
  - CBC
  - DNA Testing
  - EDTA Whole Blood
  - Fatigue
  - Genetic Carrier
  - Genetic Disorders
  - Hb Typing
  - Lab Test
  (0)
  
  Package Premium Prevention for Couple at Risk Assessment of Thalassemia
  
  ฿17,290.00
  
  Comprehensive package for thalassemia risk assessment in couples, including CBC, hemoglobin typing, and DNA tests.
  
  Add to cart
- Add to cart
  - Adults
  Package Premium Prevention for Couple at Risk Assessment of Thalassemia
  (0)
  ฿17,290.00
- - Adults
  - Blood Clots
  - Blood Clotting Disorders
  - Cardiovascular Issues
  - EDTA Whole Blood
  - Genetic Disorders
  - Lab Test
  - None
  - PCR and Direct Sequencing
  - Stroke
  (0)
  
  PAI-1 Gene Promoter Polymorphism (4G/5G)
  
  ฿8,526.00
  
  Detects the 4G/5G polymorphism in the PAI-1 gene, associated with the regulation of blood clotting and increased risk of thrombotic…
  
  Add to cart
- Add to cart
  - Adults
  PAI-1 Gene Promoter Polymorphism (4G/5G)
  (0)
  ฿8,526.00
- - Adults
  - Blood
  - Blood Clots
  - Cardiovascular Disease
  - Genetic Disorders
  - Genetic Testing
  - Lab Test
  - None
  - Stroke
  (0)
  
  PAI-1 Gene Promoter Polymorphism (4G/5G) [Quest diagnostic]
  
  ฿27,750.00
  
  A genetic test that identifies the 4G/5G polymorphism in the PAI-1 gene promoter, associated with altered risk of thrombosis and…
  
  Add to cart
- Add to cart
  - Adults
  PAI-1 Gene Promoter Polymorphism (4G/5G) [Quest diagnostic]
  (0)
  ฿27,750.00
- - All Ages
  - EDTA Whole Blood
  - Genetic Disorders
  - Hearing Loss
  - Lab Test
  - Next-Generation Sequencing (NGS)
  - None
  - Thyroid Issues
  (0)
  
  Pendred syndrome (SLC26A4) (Genome star)
  
  ฿107,100.00
  
  Detects mutations in the SLC26A4 gene associated with Pendred syndrome, a genetic disorder leading to hearing loss and thyroid dysfunction.
  
  Add to cart
- Add to cart
  - All Ages
  Pendred syndrome (SLC26A4) (Genome star)
  (0)
  ฿107,100.00
- - Adults
  - EDTA Whole Blood
  - Embryos
  - Family Planning
  - Genetic Disorders
  - Lab Test
  - N/A
  - Next-Generation Sequencing
  (0)
  
  PGT-A and PGT-M for alpha thalassemia (Family and 1st-4th embryos)
  
  ฿196,300.00
  
  Preimplantation testing for chromosomal abnormalities and genetic conditions like alpha thalassemia.
  
  Add to cart
- Add to cart
  - Adults
  PGT-A and PGT-M for alpha thalassemia (Family and 1st-4th embryos)
  (0)
  ฿196,300.00
- - Adults
  - Anemia
  - EDTA Whole Blood
  - Embryos
  - Family History
  - Fatigue
  - Genetic Disorders
  - IVF
  - Lab Test
  - NGS
  (0)
  
  PGT-A and PGT-M for Beta thalassemia (Family and 1st-4th embryos)
  
  ฿99,000.00
  
  Preimplantation testing to detect beta-thalassemia mutations in embryos for family planning.
  
  Add to cart
- Add to cart
  - Adults
  PGT-A and PGT-M for Beta thalassemia (Family and 1st-4th embryos)
  (0)
  ฿99,000.00
- - All Ages
  - Alpha Thalassemia
  - Anemia
  - EDTA Whole Blood
  - Embryo Biopsy
  - Family Planning
  - Fatigue
  - Fragment Analysis
  - Genetic Disorders
  - Indirect Genotyping
  (0)
  
  PGT-M for alpha thalassemia (Family and 1st-4th embryos)
  
  ฿207,571.00
  
  Preimplantation genetic testing for alpha thalassemia, using linked polymorphic markers to study familial alleles inheritance.
  
  Add to cart
- Add to cart
  - All Ages
  PGT-M for alpha thalassemia (Family and 1st-4th embryos)
  (0)
  ฿207,571.00
- - Beta Thalassemia
  - EDTA Whole Blood
  - Embryos
  - Genetic Disorders
  - Lab Test
  - Microsatellite Marker Analysis
  - N/A
  - None
  - Prenatal
  - Sanger Sequencing
  (0)
  
  PGT-M for Beta thalassemia (Family and 1st-4th embryos)
  
  ฿82,500.00
  
  A preimplantation genetic test that detects beta thalassemia mutations in embryos, helping families at risk of thalassemia ensure the genetic…
  
  Add to cart
- Add to cart
  - Beta Thalassemia
  PGT-M for Beta thalassemia (Family and 1st-4th embryos)
  (0)
  ฿82,500.00
- - Adults
  - EDTA Whole Blood
  - Embryos
  - Family Planning
  - Genetic Disorders
  - Lab Test
  - N/A
  - Sanger Sequencing
  - STR Analysis
  (0)
  
  PGT-M for common and rare disease by Direct Sequencing (add on embryo)
  
  ฿19,800.00
  
  Preimplantation genetic testing for mutations in embryos using Sanger sequencing and STR analysis.
  
  Add to cart
- Add to cart
  - Adults
  PGT-M for common and rare disease by Direct Sequencing (add on embryo)
  (0)
  ฿19,800.00
- - Adults
  - Assisted Reproduction
  - EDTA Whole Blood
  - Embryos
  - Family History of Genetic Disorders
  - Family Planning
  - Genetic Disorders
  - Infertility
  - IVF
  - Lab Test
  (0)
  
  PGT-M for common and rare disease by Direct Sequencing (Family and 1st-4th embryos)
  
  ฿99,000.00
  
  Preimplantation genetic testing (PGT-M) for families at risk of transmitting genetic disorders. Identifies mutations in embryos before implantation in IVF…
  
  Add to cart
- Add to cart
  - Adults
  PGT-M for common and rare disease by Direct Sequencing (Family and 1st-4th embryos)
  (0)
  ฿99,000.00
- - Adults
  - EDTA Whole Blood
  - Embryo Biopsy
  - Family History of Genetic Disorders
  - Genetic Counseling
  - Genetic Disorders
  - IVF
  - Lab Test
  - Linkage Analysis
  - Monogenic Diseases
  (0)
  
  PGT-M for common disease
  
  ฿365,781.00
  
  Identifies genetic mutations and inheritance patterns in embryos before implantation, used for families with a known risk of monogenic diseases.
  
  Add to cart
- Add to cart
  - Adults
  PGT-M for common disease
  (0)
  ฿365,781.00
- - Adults
  - Blood
  - Drug Sensitivity
  - Fever
  - Gastrointestinal Symptoms
  - Genetic Disorders
  - Genetic Testing
  - Lab Test
  - None
  - Rash
  (0)
  
  Pharmacogenetics for Abacavir (HLA-B*5701 allele)
  
  ฿4,250.00
  
  Genetic testing for the HLA-B*5701 allele, which predisposes patients to hypersensitivity reactions to abacavir, an antiretroviral drug. Identifying carriers helps…
  
  Add to cart
- Add to cart
  - Adults
  Pharmacogenetics for Abacavir (HLA-B*5701 allele)
  (0)
  ฿4,250.00

Health Checkup Packages

STD & STI Testing

Doctor On Call 24/7

PEP & PrEP — HIV Prevention

Nurse at Home

Genetic & DNA Testing

Longevity Testing by Jivi

Corporate Health Checkup

IV Drip Therapy

Plastic Surgery & Aesthetics

Lab Tests Directory

Weight Loss(GLP-1)

Newborn screening test panel

Newborn screening test panel

NIFTY Test [BGI]

NIFTY Test [BGI]

Oculopharyngeal muscular dystrophy

Oculopharyngeal muscular dystrophy

OF test for hereditary spherocytosis

OF test for hereditary spherocytosis

Package Premium Prevention for Couple at Risk Assessment of Thalassemia

Package Premium Prevention for Couple at Risk Assessment of Thalassemia

PAI-1 Gene Promoter Polymorphism (4G/5G)

PAI-1 Gene Promoter Polymorphism (4G/5G)

PAI-1 Gene Promoter Polymorphism (4G/5G) [Quest diagnostic]

PAI-1 Gene Promoter Polymorphism (4G/5G) [Quest diagnostic]

Pendred syndrome (SLC26A4) (Genome star)

Pendred syndrome (SLC26A4) (Genome star)

PGT-A and PGT-M for alpha thalassemia (Family and 1st-4th embryos)

PGT-A and PGT-M for alpha thalassemia (Family and 1st-4th embryos)

PGT-A and PGT-M for Beta thalassemia (Family and 1st-4th embryos)

PGT-A and PGT-M for Beta thalassemia (Family and 1st-4th embryos)

PGT-M for alpha thalassemia (Family and 1st-4th embryos)

PGT-M for alpha thalassemia (Family and 1st-4th embryos)

PGT-M for Beta thalassemia (Family and 1st-4th embryos)

PGT-M for Beta thalassemia (Family and 1st-4th embryos)

PGT-M for common and rare disease by Direct Sequencing (add on embryo)

PGT-M for common and rare disease by Direct Sequencing (add on embryo)

PGT-M for common and rare disease by Direct Sequencing (Family and 1st-4th embryos)

PGT-M for common and rare disease by Direct Sequencing (Family and 1st-4th embryos)

PGT-M for common disease

PGT-M for common disease

Pharmacogenetics for Abacavir (HLA-B*5701 allele)

Pharmacogenetics for Abacavir (HLA-B*5701 allele)

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