Neonatal-onset hereditary coproporphyria with male pseudohermaphrodism. [electronic resource]
Producer: 20020111Description: 3871-3 p. digitalISSN:- 0006-4971
- Adrenal Insufficiency -- complications
- Adrenocorticotropic Hormone -- blood
- Base Sequence
- Chorionic Gonadotropin
- Coproporphyrins -- analysis
- DNA -- chemistry
- Deoxyribonuclease HpaII -- metabolism
- Disorders of Sex Development -- complications
- Exons
- Feces -- chemistry
- Heterozygote
- Humans
- Hydrocortisone -- blood
- Infant, Newborn
- Karyotyping
- Male
- Molecular Sequence Data
- Mutation
- Pedigree
- Polymerase Chain Reaction
- Porphyrias, Hepatic -- complications
- Sequence Analysis, DNA
- Testosterone -- blood
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Publication Type: Case Reports; Journal Article
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