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A pregnancy test detects human chorionic gonadotropin (hCG) to determine pregnancy. Produced by the placenta after embryo implantation, hCG is detected through urine tests at home or in a doctor's office, or through blood tests in a healthcare setting.

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    Intergen Genetics and Rare Diseases Diagnosis Center, established in 1999, is dedicated to prioritizing people, life, and science. We are deeply involved in diagnosis and treatment development for genetic diseases, crafting patient-specific tests tailored to individual needs. Our services include BabySEQ (NIPT), Genetic Risk Assessment Packages, Cancer Genetic Tests, Pathology Tests, Preimplantation Genetic Diagnosis (PGD), PregnaRisk, and Whole Exome Sequencing (WES). With a commitment to advancing genetic medicine, we strive to provide personalized care and innovative solutions to patients, ensuring the highest standards of precision and effectiveness in genetic healthcare. Trust Intergen Genetics and Rare Diseases Diagnosis Center for comprehensive genetic services tailored to your unique genetic makeup.

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