Soussi-YanicostasNFaivre-SarrailhCHardelinJPLevilliersJRougonGPetitC. Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner. J Cell Sci1998; 111: 2953–65.
2.
LutzBRugarliEIEicheleGBallabioA. X-linked Kallmann syndrome. A neuronal targeting defect in the olfactory system?. FEBS Lett1993; 325: 128–34.
3.
HardelinJPJulliardAKMoniotB. Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: Implications for the developmental anomalies of X chromosome-linked Kallmann syndrome. Dev Dyn1999; 215: 26–44.
4.
OliveiraLMSeminaraSBBeranovaM. The importance of autosomal genes in Kallmann syndrome: Genotype-phenotype correlations and neuroendocrine characteristics. J Clin Endocrinol Metab2001; 86: 1532–8.
5.
RawsonNEBrandJGCowartBJ. Functionally mature olfactory neurons from two anosmic patients with Kallmann syndrome. Brain Res1995; 681: 58–64.
6.
SchwobJESzumowskiKELeopoldDAEmkoP. Histopathology of olfactory mucosa in Kallmann's syndrome. Ann Otol Rhinol Laryngol1993; 102: 117–22.
7.
MoormanJRCrainBOsborneD. Kallmann's syndrome with associated cardiovascular and intracranial anomalies. Am J Med1984; 77: 369–72.
8.
LieblichJMRogolADWhiteBJRosenSW. Syndrome of anosmia with hypogonadotropic hypogonadism (Kallmann syndrome): Clinical and laboratory studies in 23 cases. Am J Med1982; 73: 506–19.
9.
BallabioAParentiGTippettP. X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): Linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome. Hum Genet1986; 72: 237–40.
10.
GasztonyiZBarsiPCzeizelAE. Kallmann syndrome in three unrelated women and an association with femur-fibula-ulna dysostosis in one case. Am J Med Genet2000; 93: 176–80.
11.
MurphyCJinichS. Olfactory dysfunction in Down's syndrome. Neurobiol Aging1996; 17: 631–7.
12.
YamanouchiHHiratoJYokooHNakoYMorikawaANakazatoY. Olfactory bulb dysplasia: A novel subtype of neuronal migration disorder. Ann Neurol1999; 46: 783–6.
13.
BraddockSRGrafeMRJonesKL. Development of the olfactory nerve: Its relationship to the craniofacies. Teratology1995; 51: 252–6.
14.
WortsmanJHughesLF. Case report: Olfactory function in a fertile eunuch with Kallmann syndrome. Am J Med Sci1996; 311: 135–8.
15.
TruwitCLBarkovichAJGrumbachMMMartiniJJ. MR imaging of Kallmann syndrome, a genetic disorder of neuronal migration affecting the olfactory and genital systems. AJNR Am J Neuroradiol1993; 14: 827–38.
16.
YousemDMTurnerWJDLiCSnyderPJDotyRL. Kallmann syndrome: MR evaluation of olfactory system. AJNR Am J Neuroradiol1993; 14: 839–43.
