Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genes

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1984 • 4,899 citations

The Metabolic Basis of Inherited Disease.

1983 • 2,885 citations

HISTOCOMPATIBILITY TESTING, 1972

1974 • 1,267 citations

Quantitative receptor autoradiography using [3H]Ultrofilm: application to multiple benzodiazepine receptors

1982 • 529 citations

A SIMPLE MICRO CYTOTOXICITY TEST

1969 • 444 citations

The structural basis of the multiple forms of human complement component C4

1984 • 419 citations

Alkaline transfer of DNA to plastic membrane

1984 • 285 citations

Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region.

1985 • 209 citations

Genetic Mapping of the 21-Hydroxylase-Deficiency Gene within the HLA Linkage Group

1978 • 203 citations

Gene Conversion in Salt-Losing Congenital Adrenal Hyperplasia with Absent Complement C4B Protein*

1986 • 127 citations

The detection of the heterozygous carrier for congenital virilizing adrenal hyperplasia

1977 • 93 citations

Aldosterone Secretion Rate in Congenital Adrenal Hyperplasia. A Discussion of the Theories on the Pathogenesis of the Salt-losing Form of the Syndrome*

1965 • 85 citations

EXTENDED MHC HAPLOTYPES IN 21-HYDROXYLASE-DEFICIENCY CONGENITAL ADRENAL HYPERPLASIA: SHARED GENOTYPES IN UNRELATED PATIENTS

1983 • 79 citations

Molecular Genetics of the Fourth Component of Human Complement and Steroid 21‐Hydroxylase

1985 • 71 citations

Attenuated Forms of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency*

1982 • 39 citations

Adrenal 21‐Hydroxylase Cytochrome P‐450 Genes within the MHC Class III Region

1985 • 34 citations

Adrenal Disorders: II. Congenital Virilizing Adrenal Hyperplasia

1962 • 32 citations