Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans1 Department of Paediatrics, University of Cambridge, Addenbrooke's Hospital Level 8, Box 116, Cambridge CB2 2QQ, UK 2 Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Cambridge Institute for Medical Research, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK 3 Unit of Paediatric and Perinatal Epidemiology, University of Bristol, 24 Tyndall Avenue, Bristol, UK 4 Clinical and Molecular Genetics Unit, Institute of Child Health, London, UK 5 Laboratory of Developmental Genetics and Imprinting, Babraham Institute, Cambridge, UK
BMC Genetics 2005, 6:22doi:10.1186/1471-2156-6-22
Additional filesAdditional File 1: Birthweight SD score (adjusted for sex and gestational age) by combination of H19 2992/1737/3238 genotypes (for each SNP, 1 = more common homozygote, 2 = heterozygote, 3 = less common homozygote). Format: PPT Size: 29KB Download file This file can be viewed with: Microsoft PowerPoint Viewer Additional File 2: Schematic map of H19 indicating exons, SNPs published on dbSNP and also published SNPs identified by the Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory (DIL) T1Dbase http://www.t1dbase.org/cgi-bin/welcome.cgi webcite. H19 2992 is indicated by the labels rs217727 and DIL1049. Format: BMP Size: 2.1MB Download file |




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