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Prenatal diagnosis of 21-OH deficiency by DR typing with group specific primers

โœ Scribed by Noiman, S.; Altshuler, R.; Gazil, E.


Book ID
123353420
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
87 KB
Volume
34
Category
Article
ISSN
0198-8859

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Prenatal diagnosis of congenital adrenal
โœ Phyllis W. Speiser; Perrin C. White; Jacob Dupont; Deguang Zhu; Arlene B. Mercad ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Springer ๐ŸŒ English โš– 593 KB

The feasibility and accuracy of gene-specific molecular genetic diagnosis for congenital adrenal hyperplasia due to 21-hydroxylase deficiency was studied in a group of 24 pregnancies at 25% risk of carrying an affected fetus. Chorionic villus sampling was performed at 9-10 weeks' gestation. Southern