Thanatophoric dysplasia type II with encephalocele and semilobar holoprosencephaly: Insights into its pathogenesis
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33765/fullpdf
Reference31 articles.
1. FGF15 promotes neurogenesis and opposes FGF8 function during neocortical development;Borello;Neural Dev,2008
2. Patterning of frontal cortex subdivisions by Fgf17;Cholfin;Proc Natl Acad Sci USA,2007
3. Frontal cortex subdivision patterning is coordinately regulated by Fgf8, Fgf17, and Emx2;Cholfin;J Comp Neurol,2008
4. Some chondrodysplasias with short limbs: Molecular perspectives;Cohen;Am J Med Genet,2002
5. The central nervous system in the Apert syndrome;Cohen;Am J Med Genet,1990
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