Osteoglophonic dysplasia: A ‘common’ mutation in a rare disease

Sow, AJRamli, R.Latiff, ZAIchikawa, S.Gray, AKNordin, R.Abd Jabar, MNPrimuharsa Putra, SHASiar, CHEcons, MJ2015-11-022015-11-022010-08Sow, A., Ramli, R., Latiff, Z., Ichikawa, S., Gray, A., Nordin, R., … Econs, M. (2010). Osteoglophonic dysplasia: A “common” mutation in a rare disease. Clinical Genetics, 78(2), 197–198. http://doi.org/10.1111/j.1399-0004.2010.01382.xhttps://hdl.handle.net/1805/7316en-USPublisher Policydwarfismmutationsdysplasiafibroblastgrowth factorreceptorinheritedcraniofacialprognathismhypertelorismhypertrophichypoplasiacraniosynostosisOsteoglophonic dysplasia: A ‘common’ mutation in a rare diseaseArticle