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Osteogenesis imperfecta: an expanding panorama of variants. Clin Orthop 1981;159:11-25.","journal-title":"Clin Orthop"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1111\/j.1651-2227.1987.tb10519.x","article-title":"Clinical and radiological features of osteogenesis imperfecta type IVA","volume":"76","author":"Paterson, C.R.; McAllion, S.J.; Shaw, J.W.","year":"1987","unstructured":"Paterson CR, McAllion SJ, Shaw JW. Clinical and radiological features of osteogenesis imperfecta type IVA. Acta Paediatr Scand 1987;76:548-52.","journal-title":"Acta Paediatr Scand"},{"key":"ref_3","first-page":"\"p\" # \"35","article-title":"Osteogenesis imperfecta SIR,-The correspondence after my leading article","volume":"65","author":"Paterson, C.R.; McAllion, S.J.; Miller, R.","year":"1983","unstructured":"Paterson CR, McAllion SJ, Miller R. Osteogenesis imperfecta SIR,-The correspondence after my leading article (22 August, p 454) requires summary. Mr Grant Williams would place gender reassignment surgery childhood.2 Those with types IB and IVB haave overt dentinogenesis imperfecta. Type II is very severe and causes stillbirth or early neonatal death; this group is identified by us in only the very few with dominant inheritance and normal sclerae. J Bone oint Surg[BrJ 1983;65:35-9.","journal-title":"J Bone oint Surg[BrJ; 454) requires summary. Mr Grant Williams would place gender reassignment surgery childhood.2 Those with types IB and IVB haave overt dentinogenesis imperfecta. Type II is very severe and causes stillbirth or early neonatal death; this group is identified by us in only the very few with dominant inheritance and normal sclerae"},{"key":"ref_4","first-page":"227","article-title":"Risk of dominant mutation in older fathers: evidence from osteogenesis imperfecta","volume":"23","author":"Carothers, A.D.; McAllion, S.J.; Paterson, C.R.","year":"1986","unstructured":"Carothers AD, McAllion SJ, Paterson CR. Risk of dominant mutation in older fathers: evidence from osteogenesis imperfecta. J Med Genet 1986;23:227-30. at \"the bottom of the list of medical importance\" and possibly abandon it altogether in view of the current pressures on the health service. His view patients who survive the neonatal period. Patients with type III disease usually have fractures at birth and progressive deformity thereafter.","journal-title":"J Med Genet; at \"the bottom of the list of medical importance\" and possibly abandon it altogether in view of the current pressures on the health service. His view patients who survive the neonatal period. Patients with type III disease usually have fractures at birth and progressive deformity thereafter"},{"key":"ref_5","first-page":"35","article-title":"Wormian bones in osteogenesis imperfecta and other disorders","volume":"8","author":"Cremin, B.; Goodman, H.; Spranger, J.; Beighton, P.","year":"1982","unstructured":"Cremin B, Goodman H, Spranger J, Beighton P. Wormian bones in osteogenesis imperfecta and other disorders. Skeletal Radiol 1982;8:35-8."},{"key":"ref_6","first-page":"2134","article-title":"Metacarpal monphometry in adults with osteowill certainly attract support, especially from those The table shows the figures for the 773 patients genesis imperfecta","volume":"i:","author":"Paterson, C.R.","year":"1978","unstructured":"Paterson CR, Metacarpal monphometry in adults with osteowill certainly attract support, especially from those The table shows the figures for the 773 patients genesis imperfecta. 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