Congenital combined pituitary hormone deficiency attributable to a novel PROP1 mutation (467insT). [electronic resource]
Producer: 20060726Description: 491-8 p. digitalISSN:- 0334-018X
- Base Sequence
- Body Height -- drug effects
- Child
- Child, Preschool
- Dwarfism, Pituitary -- genetics
- Female
- Homeodomain Proteins -- genetics
- Hormone Replacement Therapy
- Human Growth Hormone -- therapeutic use
- Humans
- Pedigree
- Pituitary Hormones -- deficiency
- Point Mutation
- Recombinant Proteins -- therapeutic use
- Thyroid Hormones -- therapeutic use
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Publication Type: Case Reports; Journal Article
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