HLA typing of cultured amniotic cells for the prenatal diagnosis of complement C4 deficiency
- 23 April 2008
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 18 (3) , 197-200
- https://doi.org/10.1111/j.1399-0004.1980.tb00871.x
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- Hormonal Phenotype and HLA-Genotype in Families of Patients with Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)Pediatric Research, 1979
- PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) BY HLA TYPINGThe Lancet, 1979
- Two HLA-linked loci controlling the fourth component of human complement.Proceedings of the National Academy of Sciences, 1978
- Linkage between the Gene (or Genes) Controlling Synthesis of the Fourth Component of Complement and the Major Histocompatibility ComplexNew England Journal of Medicine, 1977