1. Genetic counseling for pre-gestational & prenatal periods
2. Diagnosis and treatment of Genetic diseases
3. Counseling for hereditary Genetic diseases.
4. Global screening for inborn errors of metabolism
5. Registration and long-term monitoring for Genetic diseases
6. Investigation of molecular mechanism(s) in hereditary diseases
7. Training & continuous education for persons who working in the field of medical genetics
8. International collaborations in the field of medical genetics and allied sciences
9. Neurogenetic section for the service of patiens with hereditary neurological disorder

Methods:
Fetoscope
Ultrasound
Chorionic Villi samping
Amniocentesis and Chromosome analysis
Umbillical cord blood
Indication:
1. Women are pregnant at age 34 or above
2. Women who have had children with gentics disorders that are 3. detectable by diagnosis technology.
3. Women who have had delivered multiple disorders with unknown diagnosis.High risk of Down’s syndrome, abnormality is tected by ultrasound, or the couples are thalassemia allel carriers
4. One of the parents has chromose balanced translocation.
5. Genetic disease family history that can be diagnosed.
6. Constantly miscarriage more than 3 times.

General screening
1. Congenital hypothyroidism
2. Glactosemia
3. Glucose-6-phosphatase dehydrogenase deficiency
4. Congenital adrenal hyperplasia
MS/MS screening
1. Medium-chain acyl-CoA dehydrogenase deficiency
2. Short-chain acyl-CoA dehydrogenase deficiency
3. Disorders of long-chain fatty acid oxidation
4. Carnitine transporter defect
5. Carnitine palmitoyl transferase I/II deficiency
6. Carnitine tanslocase deficiency
7. propionic acidemia
8. Methylmalonic acidemia
9. Isovaleic acidemia
10.Glutaric acidemias
11.3-hydroxy-3-methylglutaric, 3-methylcrotonyl-CoA-carboxylase deficiency
12.Maple syrup urine disease
13.Citrullinemia I/II
14.Tyrosinemia II/III
15.Argininosuccinic acidemia
16.Argininemia
17.Hyperammonemia, Hyperornithinemia, homocitrullinuria syndrome
18.Phenylketonuria
19.Hypermethionemia

After pre-marriage health screening, those who are suspects of genetic disorders or metal disease will need further tests after the pre-marriage health screening.
When maternal thalassemia screening is positive, both husband and wife need to confirm the diagnosis.
Newborn primary screening is positive, the baby and the family of the baby have to have further tests.
Genetic disease or mental disease has been suspected in immediate family or pregnant women.