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MK Hajihosseini, A Swetloff, P Ferretti… - J ANAT, 2011 - discovery.ucl.ac.uk
... Cortical and cranial nerve defects resulting from gain-of-FGF Receptor 2 (FgfR2) signalling in
an Apert syndrome mouse model. ... Type: Article. Title: Cortical and cranial nerve defects resulting
from gain-of-FGF Receptor 2 (FgfR2) signalling in an Apert syndrome mouse model. ...
Cached
[PDF] from peerproject.euM Hajihosseini, L Wheldon, N Khodabukus… - 2011 - repository.peerproject.eu
Lee M. Wheldon1 , Naila Khodabukus1, Susannah J. Patey1, Terence G. Smith,2 John K. Heath1
and Mohammad K. Hajihosseini2$ ... 1School of Biosciences, University of Birmingham,
Edgbaston, B15 2TT, UK. 2School of Biological Sciences, University of East Anglia, ...
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[HTML] from biochemj.orgL Wheldon, N Khodabukus, S Patey, T Smith… - Biochem. J, 2011 - biochemj.org
AS (Apert syndrome) is a congenital disease composed of skeletal, visceral and neural
abnormalities, caused by dominant-acting mutations in FGFR2 [FGF (fibroblast growth factor)
receptor 2]. Multiple FGFR2 splice variants are generated through alternative splicing, ...
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PKC Au, YKY Kwok, KY Leung… - Prenatal …, 2011 - Wiley Online Library
... Research Letter. Detection of the S252W mutation in fibroblast growth factor receptor
2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert
syndrome. Patrick KC Au 1,3 ,; Yvonne KY Kwok 2 ,; KY Leung ...
All 4 versions
KA Allam, DC Wan, K Khwanngern… - Plastic and …, 2011 - journals.lww.com
Wolters Kluwer Health may email you for journal alerts and information, but is committed to maintaining
your privacy and will not share your personal information without your express consent. For more
information, please refer to our Privacy Policy. ... From the Division of Plastic and ...
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