The patient with combined deficiency of neuraminidase and 21-hydroxylase

Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene.

Yasuhiro Higashi, H. Yoshioka, Miki Yamane et al. · Proceedings of the National Academy of Sciences · 1986 · 561 citations · Full text

Genuine Genes, Genetics, Molecular Biology +16

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.

Perrin C. White, Dario Grossberger, Barbara J. Onufer et al. · Proceedings of the National Academy of Sciences · 1985 · 490 citations · Full text

Human Growth, Genetics, Molecular Genetics +20

Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

Michael C. Carroll, R. Duncan Campbell, Roy Porter · Proceedings of the National Academy of Sciences · 1985 · 371 citations · Full text

Hla, Histocompatibility, Genetics +19

Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man.

Z Awdeh, D Raum, Edmond J. Yunis et al. · Proceedings of the National Academy of Sciences · 1983 · 362 citations · Full text

Hla, Histocompatibility, Genetics +16

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.

Perrin C. White, Maria I. New, Bo Dupont · Proceedings of the National Academy of Sciences · 1984 · 292 citations · Full text

Genetics, Gynecology, Defective Gene +19