{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,2]],"date-time":"2026-10-02T10:04:10Z","timestamp":1790935450238,"version":"4.1.0"},"reference-count":22,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[1992,1,1]],"date-time":"1992-01-01T00:00:00Z","timestamp":694224000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Calcif Tissue Int"],"published-print":{"date-parts":[[1992,1]]},"DOI":"10.1007\/bf00297295","type":"journal-article","created":{"date-parts":[[2004,10,6]],"date-time":"2004-10-06T13:44:05Z","timestamp":1097070245000},"page":"36-41","source":"Crossref","is-referenced-by-count":88,"title":["Osteogenesis imperfecta: A clinical study of the first ten years of life"],"prefix":"10.1007","volume":"50","author":[{"given":"U.","family":"Vetter","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"B.","family":"Pontz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E.","family":"Zauner","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R. E.","family":"Brenner","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J.","family":"Spranger","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"key":"CR1","first-page":"237","volume":"42","author":"P Byers","year":"1988","unstructured":"Byers P, Tsipouras P, Bonadia J, Starman BJ, Schwartz RC (1988) Perinatal lethal osteogenesis imperfecta (O.I. type II): a biochemically heterogenous disorder usually due to new mutations in the genes for type I collagen. Am J Hum Genet 42:237?248","journal-title":"Am J Hum Genet"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"14737","DOI":"10.1016\/S0021-9258(18)47857-X","volume":"262","author":"BE Vogel","year":"1987","unstructured":"Vogel BE, Minor RR, Freund M, Prockop DJ (1987) A point mutation in a type I procollagen gene converts glycine 748 of the ? 1 chain to cysteine and destabilizes the triple helix in a lethal variant of osteogenesis imperfecta. J Biol Chem 262:14737?14744","journal-title":"J Biol Chem"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"7734","DOI":"10.1016\/S0021-9258(18)68560-6","volume":"263","author":"RJ Wenstrup","year":"1988","unstructured":"Wenstrup RJ, Cohn DH, Cohen T, Byers P (1988) Arginine for glycine substitution in the triple helical domain of the products of one ?2 (I) collagen allele (COL1A2) produces the osteogenesis imperfecta type IV phenotype. J Biol Chem 263:7734?7740","journal-title":"J Biol Chem"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1136\/jmg.16.2.101","volume":"16","author":"DO Sillence","year":"1979","unstructured":"Sillence DO, Senn AS, Danks DM (1979) Genetic heterogeneity in osteogenesis imperfecta. J Med Gen 16:101?116","journal-title":"J Med Gen"},{"key":"CR5","first-page":"1","volume":"4","author":"P Byers","year":"1988","unstructured":"Byers P (1988) Osteogenesis imperfecta: an update. Growth, Genet Horm 4:1?5","journal-title":"Growth, Genet Horm"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"390","DOI":"10.1136\/jmg.24.7.390","volume":"24","author":"EM Thompson","year":"1987","unstructured":"Thompson EM, Young ID, Hall CM, Pembrey ME (1987) Recurrence risk and prognosis in severe sporadic osteogenesis imperfecta. J Med Gen 24:390?405","journal-title":"J Med Gen"},{"key":"CR7","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1111\/j.1399-0004.1984.tb00797.x","volume":"26","author":"D Viljoen","year":"1984","unstructured":"Viljoen D, Pearn J, Beighton P (1984) Manifestations and natural history of idiopathic hemihypertrophy: a review of eleven cases. Clin Gen 26:81?86","journal-title":"Clin Gen"},{"key":"CR8","volume-title":"The brittle bone syndrome","author":"R Smith","year":"1983","unstructured":"Smith R, Francis MJO, Houghton GR (1983) The brittle bone syndrome. Butterworth, London"},{"key":"CR9","doi-asserted-by":"crossref","first-page":"170","DOI":"10.1136\/adc.51.3.170","volume":"51","author":"JM Tanner","year":"1976","unstructured":"Tanner JM, Whitehouse RH (1976) Clinical longitudinal standards for height, height velocity, weight velocity and stages of puberty. Arch Dis Child 51:170?177","journal-title":"Arch Dis Child"},{"key":"CR10","first-page":"555","volume":"176","author":"R Smith","year":"1975","unstructured":"Smith R, Francis MJO, Bauze RJ (1975) Osteogenesis imperfecta. A clinical and biochemical study of a generalized connective tissue disorder. Quart J Med 176:555?573","journal-title":"Quart J Med"},{"key":"CR11","first-page":"3935","volume":"65","author":"CR Paterson","year":"1983","unstructured":"Paterson CR, McAllion S, Miller R (1983) Osteogenesis imperfecta with dominant inheritance and normal sclerae. J Bone Joint Surg 65B:3935?3938","journal-title":"J Bone Joint Surg"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1111\/j.1651-2227.1987.tb10519.x","volume":"76","author":"CR Paterson","year":"1987","unstructured":"Paterson CR, McAllion S, Shaw JW (1987) Clinical and radiological features of osteogenesis imperfecta type IV. Acta Paediatr Scand 76:548?552","journal-title":"Acta Paediatr Scand"},{"key":"CR13","first-page":"287","volume":"63","author":"R Wynne-Davies","year":"1981","unstructured":"Wynne-Davies R, Gromley J (1981) Clinical and genetic patterns in osteogenesis imperfecta. J Bone Jt Surg 63B:287?298","journal-title":"J Bone Jt Surg"},{"key":"CR14","doi-asserted-by":"crossref","first-page":"821","DOI":"10.1002\/ajmg.1320230309","volume":"23","author":"DO Sillence","year":"1986","unstructured":"Sillence DO, Barlow KK, Cole G, Dietrich S, Gerber AP, Rimoin DL (1986) Osteogenesis imperfecta type III. Delineation of phenotype with reference to genetic heterogeneity. Am J Med Genet 23:821?832","journal-title":"Am J Med Genet"},{"key":"CR15","doi-asserted-by":"crossref","first-page":"605","DOI":"10.1097\/01241398-198809000-00022","volume":"8","author":"TE Burke","year":"1988","unstructured":"Burke TE, Crerand SJ, Dowling F (1988) Hypertrophic callus formation leading to high-output cardiac failure in a patient with osteogenesis imperfecta. J Pediatr Orthop 8:605?610","journal-title":"J Pediatr Orthop"},{"key":"CR16","doi-asserted-by":"crossref","first-page":"199","DOI":"10.1097\/00003086-198206000-00035","volume":"166","author":"RK Beals","year":"1982","unstructured":"Beals RK (1982) Hemihypertrophy and hemihypotrophy. Clin Orth Rel Res 166:199?203","journal-title":"Clin Orth Rel Res"},{"key":"CR17","first-page":"115","volume":"7","author":"PL Lukinmaa","year":"1987","unstructured":"Lukinmaa PL, Ranta H, Ranta K (1987) Dental findings in osteogenesis imperfecta: occurrence and expression of type I dentinogenesis imperfecta. J Craniofac Genet Dev Biol 7:115?125","journal-title":"J Craniofac Genet Dev Biol"},{"key":"CR18","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1161\/01.CIR.73.1.54","volume":"73","author":"J Hortop","year":"1986","unstructured":"Hortop J, Tsipouras P, Hanley JA, Marcon BJ, Shapiro JR (1986) Cardiovascular involvement in osteogenesis imperfecta. Circulation 73:54?60","journal-title":"Circulation"},{"key":"CR19","volume-title":"Congenital diseases of the heart","author":"AM Rudolf","year":"1974","unstructured":"Rudolf AM (1974) Congenital diseases of the heart. Year Book Medical Publishers, Chicago"},{"key":"CR20","doi-asserted-by":"crossref","first-page":"184","DOI":"10.1007\/BF01958277","volume":"149","author":"U Vetter","year":"1989","unstructured":"Vetter U, Maierhofer R, Mueller M, Lang D, Teller WM, Brenner R, Frohneberg D, Woersdoerfer O (1989) Osteogenesis imperfecta in childhood: cardiac and renal manifestations. Eur J Pediatr 149:184?187","journal-title":"Eur J Pediatr"},{"key":"CR21","first-page":"100","volume":"183","author":"LE Underwood","year":"1982","unstructured":"Underwood LE, Clemmons DR, D'Ercole AJ, Minuto F, Chatelain PG, Copeland KC, van Wyk JJ (1982) Somatomedin C: measurement by radioimmunoassay and regulatory mechanisms in human subjects. Bull Swiss Acad Med 183:100?110","journal-title":"Bull Swiss Acad Med"},{"key":"CR22","doi-asserted-by":"crossref","first-page":"145","DOI":"10.1530\/acta.0.1130145","volume":"113","author":"M Binoux","year":"1986","unstructured":"Binoux M, Gourmelen M, Girard F (1986) Serum levels of insulin-like growth factor and IGF binding protein in constitutionally short children and adolescents. Acta Endocrinol 113:145?152","journal-title":"Acta Endocrinol"}],"container-title":["Calcified Tissue International"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00297295.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00297295\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00297295","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,4,29]],"date-time":"2023-04-29T13:15:27Z","timestamp":1682774127000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00297295"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1992,1]]},"references-count":22,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1992,1]]}},"alternative-id":["BF00297295"],"URL":"https:\/\/doi.org\/10.1007\/bf00297295","relation":{},"ISSN":["0171-967X","1432-0827"],"issn-type":[{"value":"0171-967X","type":"print"},{"value":"1432-0827","type":"electronic"}],"subject":[],"published":{"date-parts":[[1992,1]]}}}