Author:
Grosse-Wilde H.,Valentine-Thon E.,Vögeler U.,Passarge E.,Lorenzen F.,Sippell W. G.,Bidlingmaier F.,Knorr D.
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference31 articles.
1. HLA typing used with cultured amniotic and chorionic villus cells for early prenatal diagnosis or parentage testing without one parent's availability
2. HLA TYPING OF AMNIOTIC-FLUID CELLS APPLIED TO PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA
3. , , (1980). B Lymphocyte isolation by thrombin-nylon wool. In: (Ed.). Histocompatibility Testing 1980. Los Angeles: UCLA Press, 287–288.
4. CLOSE GENETIC LINKAGE BETWEEN HLA AND CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY)
5. (1985). Pitfalls in prenatal diagnosis of 21–hydroxylase deficiency by amniotic fluid steroid analysis? A six years experience in 102 pregnancies at risk. In: (Ed.). Congenital Adrenal Hyperplasia, Vol. 458, Annals of the New York Academy of Sciences, New York, 130–147.
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