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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 9, 2024. (Total: 231298Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Glaucoma and CHRDL1[original query]
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
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
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