Non-expression of a common mutation in the 21-hydroxylase gene: implications for prenatal diagnosis and carrier testing.

Name: Non-expression of a common mutation in the 21-hydroxylase gene: implications for prenatal diagnosis and carrier testing.
Author: Rumsby, G

Non-expression of a common mutation in the 21-hydroxylase gene: implications for prenatal diagnosis and carrier testing. — المؤلف: Rumsby, G — Journal of medical genetics 19970204

المؤلف: Rumsby, G
النشر: Journal of medical genetics 19970204
الوصف: 798-9 p.
الموضوعات: Adrenal Hyperplasia, Congenital؛ DNA Mutational Analysis؛ Disorders of Sex Development؛ Female؛ Gene Amplification؛ Genetic Carrier Screening؛ Genotype؛ Humans