Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients. [electronic resource]
Producer: 20040402Description: 1079-88 p. digitalISSN:- 0021-972X
- Adolescent
- Adult
- Child
- DNA Mutational Analysis
- Extracellular Matrix Proteins -- genetics
- Family Health
- Female
- Genetic Predisposition to Disease -- epidemiology
- Humans
- Kallmann Syndrome -- epidemiology
- Magnetic Resonance Imaging
- Male
- Middle Aged
- Nerve Tissue Proteins -- genetics
- Pedigree
- Prevalence
- Receptor Protein-Tyrosine Kinases -- genetics
- Receptor, Fibroblast Growth Factor, Type 1
- Receptors, Fibroblast Growth Factor -- genetics
- Smell
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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