PubMed (OMIM) for id: 98473

Year	Number of Results
1984	1
1989	2
1990	1
1992	1
1993	1
1994	2
1995	3
1996	2
1997	1
1998	4
1999	4
2000	5
2001	2
2002	3
2003	5
2004	5
2005	5
2024	0

1

Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1.

Kim HG, Herrick SR, Lemyre E, Kishikawa S, Salisz JA, Seminara S, MacDonald ME, Bruns GA, Morton CC, Quade BJ, Gusella JF. Kim HG, et al. J Med Genet. 2005 Aug;42(8):666-72. doi: 10.1136/jmg.2004.026989. J Med Genet. 2005. PMID: 16061567 Free PMC article. No abstract available.

2

Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly.

Jehee FS, Johnson D, Alonso LG, Cavalcanti DP, de Sá Moreira E, Alberto FL, Kok F, Kim C, Wall SA, Jabs EW, Boyadjiev SA, Wilkie AO, Passos-Bueno MR. Jehee FS, et al. Clin Genet. 2005 Jun;67(6):503-10. doi: 10.1111/j.1399-0004.2005.00438.x. Clin Genet. 2005. PMID: 15857417

3

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis.

Huang N, Pandey AV, Agrawal V, Reardon W, Lapunzina PD, Mowat D, Jabs EW, Van Vliet G, Sack J, Flück CE, Miller WL. Huang N, et al. Am J Hum Genet. 2005 May;76(5):729-49. doi: 10.1086/429417. Epub 2005 Mar 25. Am J Hum Genet. 2005. PMID: 15793702 Free PMC article.

4

Acidic fibroblast growth factor (FGF-1) and FGF receptor 1 signaling in human Y79 retinoblastoma.

Siffroi-Fernandez S, Cinaroglu A, Fuhrmann-Panfalone V, Normand G, Bugra K, Sahel J, Hicks D. Siffroi-Fernandez S, et al. Arch Ophthalmol. 2005 Mar;123(3):368-76. doi: 10.1001/archopht.123.3.368. Arch Ophthalmol. 2005. PMID: 15767480

5

Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation.

White KE, Cabral JM, Davis SI, Fishburn T, Evans WE, Ichikawa S, Fields J, Yu X, Shaw NJ, McLellan NJ, McKeown C, Fitzpatrick D, Yu K, Ornitz DM, Econs MJ. White KE, et al. Am J Hum Genet. 2005 Feb;76(2):361-7. doi: 10.1086/427956. Epub 2004 Dec 28. Am J Hum Genet. 2005. PMID: 15625620 Free PMC article.

6

Common and distinct elements in cellular signaling via EGF and FGF receptors.

Schlessinger J. Schlessinger J. Science. 2004 Nov 26;306(5701):1506-7. doi: 10.1126/science.1105396. Science. 2004. PMID: 15567848

7

PKC412 inhibits the zinc finger 198-fibroblast growth factor receptor 1 fusion tyrosine kinase and is active in treatment of stem cell myeloproliferative disorder.

Chen J, Deangelo DJ, Kutok JL, Williams IR, Lee BH, Wadleigh M, Duclos N, Cohen S, Adelsperger J, Okabe R, Coburn A, Galinsky I, Huntly B, Cohen PS, Meyer T, Fabbro D, Roesel J, Banerji L, Griffin JD, Xiao S, Fletcher JA, Stone RM, Gilliland DG. Chen J, et al. Proc Natl Acad Sci U S A. 2004 Oct 5;101(40):14479-84. doi: 10.1073/pnas.0404438101. Epub 2004 Sep 24. Proc Natl Acad Sci U S A. 2004. PMID: 15448205 Free PMC article.

8

Identification of a novel gene, FGFR1OP2, fused to FGFR1 in 8p11 myeloproliferative syndrome.

Grand EK, Grand FH, Chase AJ, Ross FM, Corcoran MM, Oscier DG, Cross NC. Grand EK, et al. Genes Chromosomes Cancer. 2004 May;40(1):78-83. doi: 10.1002/gcc.20023. Genes Chromosomes Cancer. 2004. PMID: 15034873

9

Antley-Bixler syndrome with radioulnar synostosis.

Hurley ME, White MJ, Green AJ, Kelleher J. Hurley ME, et al. Pediatr Radiol. 2004 Feb;34(2):148-51. doi: 10.1007/s00247-003-1066-7. Epub 2003 Sep 26. Pediatr Radiol. 2004. PMID: 14513299

10

FGF-23 in fibrous dysplasia of bone and its relationship to renal phosphate wasting.

Riminucci M, Collins MT, Fedarko NS, Cherman N, Corsi A, White KE, Waguespack S, Gupta A, Hannon T, Econs MJ, Bianco P, Gehron Robey P. Riminucci M, et al. J Clin Invest. 2003 Sep;112(5):683-92. doi: 10.1172/JCI18399. J Clin Invest. 2003. PMID: 12952917 Free PMC article.

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