X-Linked Megalocornea Caused by Mutations in CHRDL1 Identifies an Essential Role for Ventroptin in Anterior Segment Development-Reference-Cited by-同舟云学术

X-Linked Megalocornea Caused by Mutations in CHRDL1 Identifies an Essential Role for Ventroptin in Anterior Segment Development

Published:2012-02 Issue:2 Volume:90 Page:247-259
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Webb Tom R.,Matarin Mar,Gardner Jessica C.,Kelberman Dan,Hassan Hala,Ang Wei,Michaelides Michel,Ruddle Jonathan B.,Pennell Craig E.,Yazar Seyhan,Khor Chiea C.,Aung Tin,Yogarajah Mahinda,Robson Anthony G.,Holder Graham E.,Cheetham Michael E.,Traboulsi Elias I.,Moore Anthony T.,Sowden Jane C.,Sisodiya Sanjay M.,Mackey David A.,Tuft Stephen J.,Hardcastle Alison J.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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4. Corneal endothelial cell measurements in megalocornea;Skuta;Arch. Ophthalmol.,1983

5. X-linked megalocornea: Close linkage to DXS87 and DXS94;Chen;Hum. Genet.,1989

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