TY  - GEN
AU  - Sato,Naoko
AU  - Katsumata,Noriyuki
AU  - Kagami,Masayo
AU  - Hasegawa,Tomonobu
AU  - Hori,Naoaki
AU  - Kawakita,Setsuyo
AU  - Minowada,Shigeru
AU  - Shimotsuka,Aki
AU  - Shishiba,Yoshimasa
AU  - Yokozawa,Masato
AU  - Yasuda,Toshiyuki
AU  - Nagasaki,Keisuke
AU  - Hasegawa,Daiichiro
AU  - Hasegawa,Yukihiro
AU  - Tachibana,Katsuhiko
AU  - Naiki,Yasuhiro
AU  - Horikawa,Reiko
AU  - Tanaka,Toshiaki
AU  - Ogata,Tsutomu
TI  - 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
SN  - 0021-972X
PY  - 2004///0402
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - DNA Mutational Analysis
KW  - Extracellular Matrix Proteins
KW  - genetics
KW  - Family Health
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - epidemiology
KW  - Humans
KW  - Kallmann Syndrome
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Middle Aged
KW  - Nerve Tissue Proteins
KW  - Pedigree
KW  - Prevalence
KW  - Receptor Protein-Tyrosine Kinases
KW  - Receptor, Fibroblast Growth Factor, Type 1
KW  - Receptors, Fibroblast Growth Factor
KW  - Smell
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1210/jc.2003-030476
ER  -