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Journal Abstract Search

126 related items for PubMed ID: 25794430

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  • 3. Identification of a mutation in the WISP3 gene in three unrelated families with progressive pseudorheumatoid dysplasia.
    Yu Y, Hu M, Xing X, Li F, Song Y, Luo Y, Ma H.
    Mol Med Rep; 2015 Jul; 12(1):419-25. PubMed ID: 25738435
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  • 5. [Clinical diagnosis and WISP3 gene mutation analysis for progressive pseudorheumatoid dysplasia].
    Ye J, Zhang HW, Wang T, Cao LF, Qiu WJ, Han LS, Zhang YF, Gu XF.
    Zhonghua Er Ke Za Zhi; 2010 Mar; 48(3):194-8. PubMed ID: 20426955
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  • 6. Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia.
    Yue H, Zhang ZL, He JW.
    Bone; 2009 Apr; 44(4):547-54. PubMed ID: 19064006
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  • 10. Novel WISP3 mutations causing spondyloepiphyseal dysplasia tarda with progressive arthropathy in two unrelated Chinese families.
    Liu L, Li N, Zhao Z, Li W, Xia W.
    Joint Bone Spine; 2015 Mar; 82(2):125-8. PubMed ID: 25553839
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  • 18. WISP3 mutation associated with pseudorheumatoid dysplasia.
    Sailani MR, Chappell J, Jingga I, Narasimha A, Zia A, Lynch JL, Mazrouei S, Bernstein JA, Aryani O, Snyder MP.
    Cold Spring Harb Mol Case Stud; 2018 Feb; 4(1):. PubMed ID: 29092958
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  • 19. Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia.
    Alawbathani S, Kawalia A, Karakaya M, Altmüller J, Nürnberg P, Cirak S.
    Cold Spring Harb Mol Case Stud; 2018 Feb; 4(1):. PubMed ID: 29258992
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  • 20. Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India.
    Rai E, Mahajan A, Kumar P, Angural A, Dhar MK, Razdan S, Thangaraj K, Wise CA, Ikegawa S, Pandita KK, Sharma S.
    Sci Rep; 2016 Jun 13; 6():27684. PubMed ID: 27291587
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