Clinical application of prenatal gene diagnosis of Duchenne and Becker muscular dystrophy;

Prenatal Gene Diagnosis for the Duchenne Muscular Dystrophy Risk Fetus by Molecule Markers

Objective:To practice prenatal diagnosis on the couples at high risk of having fetus with α-thalassemia (thal).

Objective To investigate the proofs of fetal genetic material in the placentas and their distribution traits, so as to development a series detecting procedures by the non invasive prenatal diagnosis for genetic diseases.

Objective: To conduct noninvasive prenatal diagnosis in couples at risk of having child with β-thalassemia major by analyzing fetal DNA in maternal plasma.

Preventive effect of prenatal diagnosis to birth defects in 9339 cases of living birth infants;

Deletion analysis and prenatal diagnosis of 32 patients with Duchenne muscular dytrophy;

The ethical problem in the prenatal diagnosis;

Serological screening and antenatal diagnosis of patients with Down s syndrome in early pregnancy;

Analysis of down s syndrome screening and antenatal diagnosis of 3195 cases in the middle period of pregnancy;

Antenatal diagnosis is a systemic project concerning many aspects.

Gene diagnosis and clinical features of facioscapulohumeral muscular dystrophy;

Rapid gene diagnosis for commom systemic Candida infection;

Application of the BglⅡ-BlnⅠdosage test to gene diagnosis of facioscapulohumeral muscular dystrophy 1A gene;