×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
GeneticVariation
CLINVAR
Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations.
28008864
2017
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
GeneticVariation
CLINVAR
KLB , encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism.
28754744
2017
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
27502037
2016
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
Variable expressivity of pfeiffer syndrome in a family with FGFR1 p.Pro252Arg mutation.
25251565
2014
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
Mutational identification of fibroblast growth factor receptor 1 and fibroblast growth factor receptor 2 genes in craniosynostosis in Indian population.
24497711
2013
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients.
24127277
2013
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
Congenital hypogonadotropic hypogonadism during childhood: presentation and genetic analyses in 46 boys.
24204987
2013
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
GeneticVariation
CLINVAR
Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.
16764984
2006
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
FGFR1 Pfeiffer syndrome without craniosynostosis: an additional case report.
16957473
2006
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
Proline to arginine mutations in FGF receptors 1 and 3 result in Pfeiffer and Muenke craniosynostosis syndromes through enhancement of FGF binding affinity.
14613973
2004
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutation.
14564217
2003
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
12627230
2003
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
A Pro250Arg substitution in mouse Fgfr1 causes increased expression of Cbfa1 and premature fusion of calvarial sutures.
10942429
2000
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature.
10861678
2000
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome.
7795583
1995
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
CausalMutation
CLINVAR
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome.
7874169
1994
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
0.720
SusceptibilityMutation
CLINVAR