Browsing by Author Chapman, Gavin

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Issue DateTitleAuthor(s)Citation
2014Gene-environment interaction demonstrates the vulnerability of the embryonic heartChapman, Bogdan; Chapman, Gavin; Grieve, Stuart; Dunwoodie, S. L.; Harvey, Richard P; James, Alexander C; Johnson, Randall S; Lopes Floro, Kylie; OReilly, Victoria C; Preis, Jost I; Shi, Hongjun; Sparrow, D. B.; Molecular Bioscience; Molecular Bioscience; Northern Clinical School: MedicineGene-environment interaction demonstrates the vulnerability of the embryonic heart, Developmental Biology, vol.391, 1, 2014,pp 99-110
2006Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype.Sillence, David; Chapman, Gavin; Dunwoodie, Sally; Ellard, S.; Fatkin, Diane; Kusumi, K.; Sparrow, D. B.; Turnpenny, P. D.; Whittock, N. V.; Wouters, Merridee A.; Childrens Hospital Westmead: Paediatrics & Child HealthMutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype., The American Journal of Human Genetics, vol.78, 1, 2006,pp N/A-N/A
2006Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype.Sillence, David; Chapman, Gavin; Dunwoodie, Sally; Ellard, S.; Fatkin, Diane; Kusumi, K.; Sparrow, D. B.; Turnpenny, P. D.; Whittock, N. V.; Wouters, Merridee A.; Childrens Hospital Westmead: Paediatrics & Child HealthMutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype., The American Journal of Human Genetics, vol.78, 1, 2006,pp N/A-N/A
2016The promises and challenges of exome sequencing in familial, non-syndromic congenital heart diseaseBlue, Gillian; Sholler, Gary; Winlaw, David; Bosman, Alexis Gina; Chapman, Gavin; Dunwoodie, Sally; Harvey, Richard; Humphreys, David; Kirk, Edwin P.; Major, Joelene; Szot, Justin O.; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child HealthThe promises and challenges of exome sequencing in familial, non-syndromic congenital heart disease, International Journal of Cardiology, vol.230, N/A, 2016,pp 155-163