Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1). [electronic resource]
Producer: 20061025Description: 78-83 p. digitalISSN:- 0303-7207
- Adolescent
- Cleft Palate -- genetics
- Cryptorchidism -- genetics
- DNA Mutational Analysis
- Deafness -- congenital
- Dental Enamel Hypoplasia -- genetics
- Follicle Stimulating Hormone -- blood
- Genitalia, Male -- abnormalities
- Humans
- Infant
- Kallmann Syndrome -- genetics
- Karyotyping
- Luteinizing Hormone -- blood
- Male
- Mutation
- Olfaction Disorders -- congenital
- Olfactory Bulb -- abnormalities
- Pedigree
- Phenotype
- Puberty, Delayed -- genetics
- Receptor, Fibroblast Growth Factor, Type 1 -- genetics
- Syndactyly -- genetics
- Synkinesis -- congenital
- Testosterone -- blood
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.