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.
Sato, Naoko
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] - The Journal of clinical endocrinology and metabolism Mar 2004 - 1079-88 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0021-972X
10.1210/jc.2003-030476 doi
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
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] - The Journal of clinical endocrinology and metabolism Mar 2004 - 1079-88 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0021-972X
10.1210/jc.2003-030476 doi
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