Citations for
1FGFR1, OGD
Osteoglophonic dysplasia: A 'common' mutation in a rare disease.
Sow AJ, Ramli R, Latiff ZA, Ichikawa S, Gray AK, Nordin R, Abd Jabar MN, Primuharsa Putra SH, Siar CH, Econs MJ.
Clin Genet 78(2):197-8. Epub 2010 Mar 5. No abstract available. PMID: 20236123 2010
2FGFR1, OGD
Extended mutational analyses of FGFR1 in osteoglophonic dysplasia.
Farrow EG, Davis SI, Mooney SD, Beighton P, Mascarenhas L, Gutierrez YR, Pitukcheewanont P, White KE.
Am J Med Genet A 140(5):537-9. No abstract available. 2006
3FGFR1, OGD
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.
Am J Hum Genet 76(2):361-7. Epub 2004 Dec 28. 2005
4OGD
Osteoglophonic dysplasia.
Greenberg F, Lewis RA.
J Med Genet 27(3):213. No abstract available. 1990