Localization of the human CYP17 gene (cytochrome P45017α) to 10q24.3 by fluorescence in situ hybridization and simultaneous chromosome banding
- 31 December 1992
- Vol. 14 (4) , 1110-1111
- https://doi.org/10.1016/s0888-7543(05)80140-5
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Isolation, characterization, and chromosomal mapping of mouse P450 17α-hydroxylase/C17–20 lyaseGenomics, 1991
- 17α-Hydroxylase/17,20-Lyase Deficiency: From Clinical Investigation to Molecular Definition*Endocrine Reviews, 1991
- The 1990 catalog of mapped genes and report of the nomenclature committee (Part 1 of 3)Cytogenetic and Genome Research, 1990
- Molecular Biology of Steroid Hormone Synthesis*Endocrine Reviews, 1988
- Structural Characterization of Normal and Mutant Human Steroid 17α- Hydroxylase Genes: Molecular Basis of One Example of Combined 17α- Hydroxylase/17,20 Lyase DeficiencyMolecular Endocrinology, 1988
- Cloning and Sequence of the Human Gene for P450cl7 (Steroid 17α-Hydroxylase/17,20 Lyase): Similarity with the Gene for P450c21DNA, 1987
- Characterization of Complementary Deoxyribonucleic Acid for Human Adrenocortical 17α-Hydroxylase: A Probe for Analysis of 17α-Hydroxylase Deficiency*Molecular Endocrinology, 1987
- Expression of Bovine 17α-Hydroxylase Cytochrome P-450 cDNA in Nonsteroidogenic (COS 1) CellsScience, 1986
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1984
- Report of the committee on the genetic constitution of chromosomes 10, 11, and 12Cytogenetic and Genome Research, 1984