[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, ... Related articles
[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, ... Related articles - Cached - All 6 versions
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 ... Related articles - All 4 versions
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