TY  - GEN
AU  - Schneider,P M
AU  - Carroll,M C
AU  - Alper,C A
AU  - Rittner,C
AU  - Whitehead,A S
AU  - Yunis,E J
AU  - Colten,H R
TI  - Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants
SN  - 0021-9738
PY  - 1986///1008
KW  - Adrenal Hyperplasia, Congenital
KW  - genetics
KW  - Alleles
KW  - Celiac Disease
KW  - Chromosome Aberrations
KW  - Chromosome Deletion
KW  - Complement C4
KW  - DNA
KW  - DNA Restriction Enzymes
KW  - Deoxyribonucleases, Type II Site-Specific
KW  - Genes
KW  - Haploidy
KW  - Humans
KW  - Major Histocompatibility Complex
KW  - Multiple Sclerosis
KW  - Nucleic Acid Hybridization
KW  - Phenotype
KW  - Polymorphism, Genetic
KW  - Steroid 21-Hydroxylase
KW  - Steroid Hydroxylases
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1172/JCI112623
ER  -