HuGE Literature Finder
Records
1
-
2
First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype-Genotype Association. Journal of clinical medicine 2022 1 11 (1): . Stingl Julia V, Diederich Stefan, Diel Heidi, Schuster Alexander K, Wagner Felix M, Chronopoulos Panagiotis, Aghayeva Fidan, Grehn Franz, Winter Jennifer, Schweiger Susann, Hoffmann Esther |
Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness. PloS one 2014 9 (8): e104163. Davidson Alice E, Cheong Sek-Shir, Hysi Pirro G, Venturini Cristina, Plagnol Vincent, Ruddle Jonathan B, Ali Hala, Carnt Nicole, Gardner Jessica C, Hassan Hala, Gade Else, Kearns Lisa, Jelsig Anne Marie, Restori Marie, Webb Tom R, Laws David, Cosgrove Michael, Hertz Jens M, Russell-Eggitt Isabelle, Pilz Daniela T, Hammond Christopher J, Tuft Stephen J, Hardcastle Alison |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 31, 2023
- Content source: