rs121909627
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
C
0.700
CausalMutation
CLINVAR
Variable expressivity of pfeiffer syndrome in a family with FGFR1 p.Pro252Arg mutation.
25251565
2014
rs121909627
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
C
0.700
CausalMutation
CLINVAR
Mutational identification of fibroblast growth factor receptor 1 and fibroblast growth factor receptor 2 genes in craniosynostosis in Indian population.
24497711
2013
rs121909627
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
C
0.700
CausalMutation
CLINVAR
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients.
24127277
2013
rs121909627
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
C
0.700
CausalMutation
CLINVAR
FGFR1 Pfeiffer syndrome without craniosynostosis: an additional case report.
16957473
2006
rs121909627
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
C
0.700
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
rs121909627
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
C
0.700
CausalMutation
CLINVAR
The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutation.
14564217
2003
rs121909627
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
C
0.700
CausalMutation
CLINVAR
Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature.
10861678
2000
rs121909627
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
C
0.700
CausalMutation
CLINVAR
A Pro250Arg substitution in mouse Fgfr1 causes increased expression of Cbfa1 and premature fusion of calvarial sutures.
10942429
2000
rs121909627
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
C
0.700
CausalMutation
CLINVAR
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome.
7795583
1995
rs121909627
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
Kallmann Syndrome 2 (disorder)
C
0.700
CausalMutation
CLINVAR
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome.
7874169
1994