Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants. [electronic resource]
Producer: 19861008Description: 650-7 p. digitalISSN:- 0021-9738
- Adrenal Hyperplasia, Congenital -- genetics
- Alleles
- Celiac Disease -- genetics
- Chromosome Aberrations
- Chromosome Deletion
- Complement C4 -- genetics
- DNA -- genetics
- DNA Restriction Enzymes
- Deoxyribonucleases, Type II Site-Specific
- Genes
- Haploidy
- Humans
- Major Histocompatibility Complex
- Multiple Sclerosis -- genetics
- Nucleic Acid Hybridization
- Phenotype
- Polymorphism, Genetic
- Steroid 21-Hydroxylase -- genetics
- Steroid Hydroxylases -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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