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Human Heredity|July 1, 1996
Identification of a polymorphic CA repeat in the COL6A2 gene on human chromosome 21q22.3P Comeglio, B Saitta, G Pepe, et al.Human Mutation|August 29, 2001
Detection of six novel FBN1 mutations in British patients affected by Marfan syndromeP Comeglio, A L Evans, G W Brice, et al.Human Mutation|December 19, 2001
Erratum: Detection of six novel FBN1 mutations in British patients affected by Marfan syndromeP Comeglio, A L Evans, G W Brice, et al.Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Neonatal Marfan syndrome caused by an exon 25 mutation of the fibrillin-1 geneN H Elçioglu, F Akalin, M Elçioglu, et al.Eye (London, England)|October 7, 2006
The -174G/C interleukin-6 promoter polymorphism influences the development of macular oedema following uncomplicated phacoemulsification surgeryI Masood, A Negi, S A Vernon, et al.The British Journal of Ophthalmology|November 26, 2002
Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitusP Comeglio, A L Evans, G Brice, et al.Neuroscience|January 18, 2015
Fibroblast growth factor and endothelin-1 receptors mediate the response of human striatal precursor cells to hypoxiaS Ambrosini, E Sarchielli, P Comeglio, et al.Prostaglandins, Leukotrienes, and Essential Fatty Acids|July 1, 1995
Platelet activation and platelet lipid composition in pulmonary cancerD Prisco, R Paniccia, M Coppo, et al.Genetic Counseling (Geneva, Switzerland)|November 11, 2008
Scoliosis, blindness and arachnodactyly in a large Turkish family: is it a new syndrome?M Dundar, K Erkilic, M Argun, et al.Haemostasis|November 1, 1995
Clottable to immunological fibrinogen ratio in plasma from control subjects and hyperfibrinogenemic patientsD Prisco, N Zarone, A A Liotta, et al.Pageof 4