Congenital 21-hydroxylase deficiency as a new deletion mutation. Detection in a proband during subsequent prenatal diagnosis by HLA typing and DNA analysis

Biochemistry, Genetics and Molecular Biology

• Nested Gene 100%
• DNA Analysis 100%
• 21-Hydroxylase 50%
• Mutation 50%
• Haplotype 50%
• Inheritance 50%
• Peripheral Blood Lymphocyte 50%
• Chromosome 6 50%
• Proband 50%
• HLA Typing 50%
• Probe 50%
• Histocompatibility 50%
• Genetic Marker 50%
• Paternity 50%