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Journal Abstract Search

139 related items for PubMed ID: 35978537

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  • 26. [Pathologic anatomy of osteogenesis imperfecta. Light and electron microscopic studies of supportive tissue and skin].
    Stöss H.
    Veroff Pathol; 1990; 134():1-88. PubMed ID: 2385955
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  • 27. Pamidronate Response in a Novel Biallelic CREB3L1 Gene Mutation-Associated Osteogenesis Imperfecta: A Case Report.
    Selina A, Kandagaddala M, Madhuri V.
    JBJS Case Connect; 2024 Jul 01; 14(3):. PubMed ID: 39058796
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  • 29. Multiexon deletions in the type I collagen COL1A2 gene in osteogenesis imperfecta type IB. Molecules containing the shortened alpha2(I) chains show differential incorporation into the bone and skin extracellular matrix.
    Mundlos S, Chan D, Weng YM, Sillence DO, Cole WG, Bateman JF.
    J Biol Chem; 1996 Aug 30; 271(35):21068-74. PubMed ID: 8702873
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  • 30. The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations.
    Joeng KS, Lee YC, Jiang MM, Bertin TK, Chen Y, Abraham AM, Ding H, Bi X, Ambrose CG, Lee BH.
    Hum Mol Genet; 2014 Aug 01; 23(15):4035-42. PubMed ID: 24634143
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  • 31. Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment.
    Fiscaletti M, Biggin A, Bennetts B, Wong K, Briody J, Pacey V, Birman C, Munns CF.
    Bone; 2018 May 01; 110():66-75. PubMed ID: 29382611
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  • 33. COL1A1 mutation analysis in Lithuanian patients with osteogenesis imperfecta.
    Benusiené E, Kucinskas V.
    J Appl Genet; 2003 May 01; 44(1):95-102. PubMed ID: 12590186
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  • 34. A family with homozygous and heterozygous p.Gly337Ser mutations in COL1A2.
    Udomchaiprasertkul W, Kuptanon C, Porntaveetus T, Shotelersuk V.
    Eur J Med Genet; 2020 Jun 01; 63(6):103896. PubMed ID: 32081708
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  • 37. Intracranial aneurysm as a possible complication of osteogenesis imperfecta: a case series and literature review.
    Matsushiro M, Harada D, Ueyama K, Kashiwagi H, Ishiura Y, Yamada H, Seino Y.
    Endocr J; 2023 Jul 28; 70(7):697-702. PubMed ID: 37164684
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  • 38. Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta.
    Zhang H, Yue H, Wang C, Hu W, Gu J, He J, Fu W, Hu Y, Li M, Zhang Z.
    Mol Med Rep; 2016 Nov 28; 14(5):4918-4926. PubMed ID: 27748872
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