Clinical and Biochemical Phenotype Across the Genotypic Spectrum of 21-hydroxylase Deficiency in 457 Individuals.
Saved in:
| Title: | Clinical and Biochemical Phenotype Across the Genotypic Spectrum of 21-hydroxylase Deficiency in 457 Individuals. |
|---|---|
| Authors: | Lao Q; Department of Pediatrics, National Institutes of Health Clinical Center, Bethesda, MD 20892, USA., Schulman A; Department of Pediatrics, National Institutes of Health Clinical Center, Bethesda, MD 20892, USA., Kulkarni S; Department of Pediatrics, National Institutes of Health Clinical Center, Bethesda, MD 20892, USA., Kollender S; Department of Pediatrics, National Institutes of Health Clinical Center, Bethesda, MD 20892, USA., Bick D; Department of Pediatrics, National Institutes of Health Clinical Center, Bethesda, MD 20892, USA., Moon A; Department of Pediatrics, National Institutes of Health Clinical Center, Bethesda, MD 20892, USA., Burkardt D; Department of Pediatrics, National Institutes of Health Clinical Center, Bethesda, MD 20892, USA.; Division of Genetics and Metabolism, Children's National Hospital, Washington, DC 20010, USA.; Department of Pediatrics and Orthopedics, George Washington University, Washington, DC 20052, USA., Merke DP; Department of Pediatrics, National Institutes of Health Clinical Center, Bethesda, MD 20892, USA.; Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD 20892, USA. |
| Source: | The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2026 Mar 17; Vol. 111 (4), pp. 1098-1113. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Oxford University Press Country of Publication: United States NLM ID: 0375362 Publication Model: Print Cited Medium: Internet ISSN: 1945-7197 (Electronic) Linking ISSN: 0021972X NLM ISO Abbreviation: J Clin Endocrinol Metab Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
Be the first to leave a comment!
