Browsing Öksüz Yayınlar Koleksiyonu - WoS by Department "Univ Connecticut, Ctr Hlth, Dept Surg, Surg Res Ctr,Mol Ophthalm Genet Lab, Framingham, CT USA -- Cumhuriyet Univ, Dept Med Biol, Sivas, Turkey -- Cumhuriyet Univ, Dept Genet, Sivas, Turkey -- Cumhuriyet Univ, Dept Ophthalmol, Sivas, Turkey -- Hosp Sick Children, Res Inst, Program Dev Biol, Toronto, ON, Canada -- Hosp Sick Children, Res Inst, Genet Program, Toronto, ON, Canada -- Univ Toronto, Dept Pediat, Toronto, ON, Canada -- Univ Toronto, Dept Mol & Med Genet, Toronto, ON, Canada -- UCL, Inst Child Hlth, Dev Biol Unit, London WC1E 6BT, England -- Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada -- Univ Alberta, Dept Med Genet, Edmonton, AB, Canada -- McGill Univ, Montreal Childrens Hosp, Ctr Hosp, Dept Pathol, Montreal, PQ, Canada -- McGill Univ, Montreal Childrens Hosp, Ctr Hosp, Dept Human Genet, Montreal, PQ, Canada -- Univ Toronto, Dept Anat & Cell Biol, Toronto, ON, Canada -- Ankara Hosp, Ophthalmol Clin, Ankara, Turkey -- Cleveland Clin Fdn, Div Ophthalmol, Ctr Genet Eye Dis, Dept Pediat, Cleveland, OH USA"
Now showing items 1-1 of 1
-
Human microphthalmia associated with mutations in the retinal homeobox gene CHX10
(NATURE PUBLISHING GROUP, 2000)Isolated human microphthalmia/anophthalmia, a cause of congenital blindness, is a clinically and genetically heterogeneous developmental disorder characterized by a small eye and other ocular abnormalities. Three ...