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1 he expression of molecules involved in human Kallmann syndrome.
2 n implicated in FGF signaling and mutated in Kallmann syndrome.
3 ystem leads to hypogonadotropic gonadism and Kallmann syndrome.
4 idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
5  semaphorin 3E (SEMA3E) in two brothers with Kallmann syndrome.
6 luding Fraser, renal cysts and diabetes, and Kallmann syndromes.
7 ed in DM, but not sIBM, were interleukin 22, Kallmann syndrome 1 (KAL-1), an adhesion molecule shown
8  receptor gene GNRHR (R262Q), and one in the Kallmann syndrome 1 sequence gene KAL1 (V371I).
9  anosmia, are reminiscent of the symptoms of Kallmann syndrome, a human developmental disease that ca
10  new genetic aetiology for Moebius syndrome, Kallmann syndrome and cyclic vomiting.
11 facial or multi-system malformations include Kallmann syndrome and idiopathic hypogonadotropic hypogo
12 er important insight into the development of Kallmann syndrome and provide tools for elucidating muta
13 d t(10;12) translocation from a subject with Kallmann syndrome and scanning genes in its vicinity in
14  corpus callosum agenesis, Joubert syndrome, Kallmann syndrome, and horizontal gaze palsy with progre
15                                        While Kallmann syndrome-associated mutations have been identif
16                  Mutations in PROKR2 lead to Kallmann syndrome, characterized by anosmia and hypogona
17 fect of GnRH in GnRH-deficient patients with Kallmann syndrome, GnRH pulses caused minimal secretory
18  expand the TUBB3 E410K phenotype to include Kallmann syndrome (hypogonadotropic hypogonadism and ano
19  this issue, we studied 2 families, one with Kallmann syndrome (IHH and anosmia) and another with nor
20                                              Kallmann syndrome is a neurological disorder characteriz
21                                              Kallmann syndrome is an inherited deficiency of gonadotr
22                WDR11, a gene associated with Kallmann syndrome, is important in reproductive system d
23             In a patient diagnosed with both Kallmann syndrome (KS) and intellectual disability (ID),
24                          CHARGE syndrome and Kallmann syndrome (KS) are two distinct developmental di
25                                              Kallmann syndrome (KS) is a congenital disorder characte
26                                              Kallmann syndrome (KS) is a genetic disease characterize
27                                      Because Kallmann syndrome (KS) is characterized by abnormal GnRH
28            Mutations in KAL1 and FGFR1 cause Kallmann syndrome (KS), whereas mutations in the GNRHR a
29 in semaphorin 3E (SEMA3E) in 2 brothers with Kallmann syndrome (KS), which causes inherited GnRH defi
30      Disruption of this migration results in Kallmann syndrome (KS), which is characterized by anosmi
31 otropic hypogonadism (nIHH) or with anosmia [Kallmann syndrome (KS)].
32 ncy, which is often associated with anosmia (Kallmann syndrome, KS).
33 onadotropic hypogonadism (IHH) with anosmia (Kallmann syndrome; KS) or with a normal sense of smell (
34 ct olfaction and sexual development, such as Kallmann syndrome, may be in part neurocristopathies.
35 for understanding the mechanism of action of Kallmann syndrome mutations and the order of trans-phosp
36 tions in CHD7 have also been reported in the Kallmann syndrome (olfactory dysfunction, delayed pubert
37 approximately 600 individuals who had either Kallmann syndrome or isolated or syndromic ocular and/or
38 m, which may be associated with anosmia (the Kallmann syndrome) or with a normal sense of smell, is a
39                        In a human condition, Kallmann syndrome, the data show a clear, indirect genet
40 pathic hypogonadotropic hypogonadism and the Kallmann syndrome was noted after discontinuation of tre
41 omal recessive) with an anosmic form of IGD (Kallmann syndrome) with loss-of-function mutations in TC