A cross-sectional multicenter study of osteogenesis imperfecta in North America - results from the linked clinical research centers
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Epigenetic detection of human chromosome 14 uniparental disomy
Murphy, S.K., Wylie, A.A., Coveler, K.J., Cotter, P.D., Papenhausen, P.R., Sutton, V.R., Shaffer, L.G., Jirtle, R.L.
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TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis
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Published in The New England journal of medicine (22.01.2015)
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Cesarean delivery is not associated with decreased at-birth fracture rates in osteogenesis imperfecta
Bellur, S., Jain, M., Cuthbertson, D., Krakow, D., Shapiro, J.R., Steiner, R.D., Smith, P.A., Bober, M.B., Hart, T., Krischer, J., Mullins, M., Byers, P.H., Pepin, M., Durigova, M., Glorieux, F.H., Rauch, F., Sutton, V.R., Lee, B., Nagamani, S.C.
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Published in Genetics in medicine (01.06.2016)
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Impact of elosulfase alfa on pain in patients with Morquio syndrome type A
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Lack of apoptosis of Sézary cells in the circulation following oral bexarotene therapy
Brennand, S., Sutton, V.R., Biagi, J., Trapani, J.A., Westerman, D., McCormack, C.J., Seymour, J.F., Kennedy, G., Prince, H.M.
Published in British journal of dermatology (1951) (01.06.2005)
Published in British journal of dermatology (1951) (01.06.2005)
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