Neurologic and ocular phenotype in Pitt-Hopkins syndrome and a zebrafish model
Page 1 of 1
Neurologic and ocular phenotype in Pitt-Hopkins syndrome and a zebrafish model
Jon Moulton Fri May 06, 2011 10:24 am
Brockschmidt A, Filippi A, Charbel Issa P, Nelles M, Urbach H, Eter N, Driever W, Weber RG. Neurologic and ocular phenotype in Pitt-Hopkins syndrome and a zebrafish model.. Hum Genet. 2011 May 5. [Epub ahead of print]
Jon Moulton- Posts : 5721
Join date : 2010-03-12
Age : 61
Location : Philomath, Oregon, USA -
Similar topics» Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome
» A zebrafish model of Axenfeld-Rieger Syndrome reveals that pitx2 regulation by retinoic acid is essential for ocular and craniofacial development
» Zebrafish cdc6 hypomorphic mutation causes Meier-Gorlin syndrome-like phenotype
» Restoration of polr1c in early embryogenesis rescues the Type 3 Treacher Collins Syndrome facial malformation phenotype in zebrafish
» Role of Chd7 in Zebrafish: A Model for CHARGE Syndrome
» A zebrafish model of Axenfeld-Rieger Syndrome reveals that pitx2 regulation by retinoic acid is essential for ocular and craniofacial development
» Zebrafish cdc6 hypomorphic mutation causes Meier-Gorlin syndrome-like phenotype
» Restoration of polr1c in early embryogenesis rescues the Type 3 Treacher Collins Syndrome facial malformation phenotype in zebrafish
» Role of Chd7 in Zebrafish: A Model for CHARGE Syndrome
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum|
|
|