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4. Osteogenesis imperfecta type VI: a form of brittle bone disease with a mineralization defect. Glorieux FH; Ward LM; Rauch F; Lalic L; Roughley PJ; Travers R J Bone Miner Res; 2002 Jan; 17(1):30-8. PubMed ID: 11771667 [TBL] [Abstract][Full Text] [Related]
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11. Evidence that abnormal high bone mineralization in growing children with osteogenesis imperfecta is not associated with specific collagen mutations. Roschger P; Fratzl-Zelman N; Misof BM; Glorieux FH; Klaushofer K; Rauch F Calcif Tissue Int; 2008 Apr; 82(4):263-70. PubMed ID: 18311573 [TBL] [Abstract][Full Text] [Related]
12. Update on the evaluation and treatment of osteogenesis imperfecta. Harrington J; Sochett E; Howard A Pediatr Clin North Am; 2014 Dec; 61(6):1243-57. PubMed ID: 25439022 [TBL] [Abstract][Full Text] [Related]
13. Osteogenesis imperfecta and its molecular diagnosis by determination of mutations of type I collagen genes. Tedeschi E; Antoniazzi F; Venturi G; Zamboni G; Tatò L Pediatr Endocrinol Rev; 2006 Sep; 4(1):40-6. PubMed ID: 17021582 [TBL] [Abstract][Full Text] [Related]
14. Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients. Hartikka H; Kuurila K; Körkkö J; Kaitila I; Grénman R; Pynnönen S; Hyland JC; Ala-Kokko L Hum Mutat; 2004 Aug; 24(2):147-54. PubMed ID: 15241796 [TBL] [Abstract][Full Text] [Related]
15. Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta. Lee KS; Song HR; Cho TJ; Kim HJ; Lee TM; Jin HS; Park HY; Kang S; Jung SC; Koo SK Hum Mutat; 2006 Jun; 27(6):599. PubMed ID: 16705691 [TBL] [Abstract][Full Text] [Related]
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