EXTENDED MHC HAPLOTYPES IN 21-HYDROXYLASE-DEFICIENCY CONGENITAL ADRENAL HYPERPLASIA: SHARED GENOTYPES IN UNRELATED PATIENTS
- 1 January 1983
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 321 (8317) , 152-156
- https://doi.org/10.1016/s0140-6736(83)92757-5
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Further evidence for different allelic variants at the 21-hydroxylase locusClinical Immunology and Immunopathology, 1982
- Gene mapping within the T/t complex of the mouse. I. t-lethal genes are nonallelicCell, 1982
- Intra-HLA recombinations localizing the 21-hydroxylase deficiency gene within the HLA complexHuman Immunology, 1981
- Location of the gene for 21-hydroxylase deficiency.Journal of Medical Genetics, 1980
- Linkage and association between HLA and 21-hydroxylase deficiency.Journal of Medical Genetics, 1980
- Genetic polymorphism of human complement C4 and detection of heterozygotesNature, 1979
- International System for Human Gene Nomenclature (1979) ISGN (1979)Cytogenetic and Genome Research, 1979
- Genetic Mapping of the 21-Hydroxylase-Deficiency Gene within the HLA Linkage GroupNew England Journal of Medicine, 1978
- Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.The Journal of Experimental Medicine, 1976
- A New Antibody Specificity, Anti‐Rga, Reacting with a Red Cell and Serum AntigenVox Sanguinis, 1976