Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations-Reference-Cited by-同舟云学术

Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations

Published:2009-06-10 Issue:12 Volume:17 Page:1527-1539
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Tümer Zeynep,Bach-Holm Daniella

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg200993.pdf

Reference71 articles.

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4. Sim KT, Krri B, Kaye SB : Posterior embryotoxon may not be a forme fruste of Axenfeld–Rieger's syndrome. J AAPOS 2004; 8: 504–506.

5. Burian HM, Rice MH, Allen L : External visibility of the Schlemm's canal. Arch Ophthalmol 1957; 57: 651–658.

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