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Fibroblast growth factor receptor 2
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#	Item
1	FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models Neus Martı´nez-Abadı´as1, Yann Heuze´1, Yingli Wang2, Ethylin Wang Jab Add to Reading List Source URL: www.getahead.psu.edu Language: English - Date: 2011-10-31 13:35:56 Anatomy Genodermatoses Tyrosine kinase receptors Fibroblast growth factor receptor 2 Apert syndrome Crouzon syndrome Craniosynostosis Fibroblast growth factor Neurocranium Health Biology Syndromes
2	Brain phenotypes in two FGFR2 mouse models for Apert syndrome Add to Reading List Source URL: www.getahead.psu.edu Language: English - Date: 2010-02-16 13:17:22 Biology Genodermatoses Apert syndrome Craniosynostosis Fibroblast growth factor receptor 2 Corpus callosum Suture Ventriculomegaly Health Anatomy Syndromes
3	DEVELOPMENTAL DYNAMICS 239:3058–3071, 2010 a PATTERNS & PHENOTYPES Add to Reading List Source URL: www.getahead.psu.edu Language: English - Date: 2010-10-27 13:48:41 Syndromes Congenital disorders Skull Genodermatoses Craniosynostosis Apert syndrome Fibroblast growth factor receptor 2 Saethre-Chotzen syndrome Suture Health Anatomy Human anatomy
4	November 6, 2014 Dear Colleagues, Please find below details of a high priority clinical study just opened to patient accrual at Northwestern Medicine Developmental Therapeutics Institute (NMDTI). A Phase 2, randomized, Add to Reading List Source URL: dti.nm.org Language: English - Date: 2014-11-06 17:29:54 Design of experiments Science Breast cancer Metastatic breast cancer Health Clinical trial Fibroblast growth factor receptor Medicine Ribbon symbolism Clinical research
5	Disease Contact details Regional Genetics Service Level 5/6, Barclay House 37 Queen Square London, WC1N 3BH Add to Reading List Source URL: www.rapid.nhs.uk Language: English - Date: 2015-03-20 10:07:30 Genodermatoses Apert syndrome Fibroblast growth factor receptor 2 Craniosynostosis Syndactyly Prenatal diagnosis Medical genetics Pregnancy Ethylenediaminetetraacetic acid Medicine Health Syndromes
6	Disease Contact details Regional Genetics Service Level 5/6, Barclay House 37 Queen Square London, WC1N 3BH Add to Reading List Source URL: www.rapid.nhs.uk Language: English - Date: 2015-03-20 10:07:31 Rare diseases Fibroblast growth factor receptor 2 Antley-Bixler syndrome Craniosynostosis Medical genetics Apert syndrome Health Medicine Syndromes
7	Network approaches to understanding mechanisms of polygenic susceptibility to cancer Principal Investigators: Bruce Ponder (Dept of Oncology, CRUK Cambridge Institute) email: [removed] Julio Saez-Rodrig Add to Reading List Source URL: www.ebi.ac.uk Language: English - Date: 2014-08-06 09:21:33 Ribbon symbolism DNA Genetic genealogy Molecular biology Single-nucleotide polymorphism Breast cancer Cancer Fibroblast growth factor receptor 2 Personalized medicine Biology Medicine Genetics
8	a guide to understanding apert syndrome a publication of children’s craniofacial association Add to Reading List Source URL: www.ccakids.org Language: English - Date: 2013-05-30 16:44:12 Genodermatoses Apert syndrome Rare diseases Congenital disorders Craniosynostosis Syndactyly Craniofacial team Fibroblast growth factor receptor 2 Cleft lip and palate Health Medicine Syndromes
9	FGFR2 Gene Mutation Analysis Interpretation Order Form Add to Reading List Source URL: www.asperbio.com Language: English - Date: 2013-08-28 08:18:16 Craniosynostosis Biology Fibroblast growth factor receptor 2 Screening Syndromes Medicine Health Prenatal diagnosis
10	a guide to understanding apert Add to Reading List Source URL: www.ccakids.com Language: English - Date: 2013-05-30 16:44:12 Genodermatoses Apert syndrome Rare diseases Congenital disorders Craniosynostosis Syndactyly Craniofacial team Fibroblast growth factor receptor 2 Cleft lip and palate Health Medicine Syndromes