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Journal Abstract Search

169 related items for PubMed ID: 8256816

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  • 3. Identical twins with the classical form of Schwartz-Jampel syndrome.
    Pinto-Escalante D, Ceballos-Quintal JM, Canto-Herrera J.
    Clin Dysmorphol; 1997 Jan; 6(1):45-9. PubMed ID: 9018418
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  • 4. Schwartz-Jampel syndrome: three pediatric case reports.
    Yapicioğlu H, Satar M, Yildizdaş D, Narli N, Suleymanova D, Tutak E.
    Genet Couns; 2003 Jan; 14(3):353-8. PubMed ID: 14577682
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  • 5. [Schwartz-Jampel syndrome (osteochondromuscular dystrophy)].
    Ben Becher S, el Mabrouk J, Debbiche A, Hammou A, Ghram N, Makni S, Boudhina T.
    Arch Fr Pediatr; 1992 Nov; 49(9):799-802. PubMed ID: 1300968
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  • 6. Chondrodystrophic myotonia (Schwartz-Jampel syndrome): report of a new case and follow-up of patients initially reported in 1969.
    Edwards WC, Root AW.
    Am J Med Genet; 1982 Sep; 13(1):51-6. PubMed ID: 7137221
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  • 12. Heterogeneity in Schwartz-Jampel chondrodystrophic myotonia.
    Giedion A, Boltshauser E, Briner J, Eich G, Exner G, Fendel H, Kaufmann L, Steinmann B, Spranger J, Superti-Furga A.
    Eur J Pediatr; 1997 Mar; 156(3):214-23. PubMed ID: 9083764
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  • 13. Extending the spectrum of distal arthrogryposis.
    Gripp KW, Scott CI, Brockett BC, Nicholson L, Mackenzie WG.
    Am J Med Genet; 1996 Nov 11; 65(4):286-90. PubMed ID: 8923937
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  • 15. [Clinical and genetic features of Schwartz-Jampel syndrome in a Chinese child: case report and literature review].
    Dai L, Fang F, Huang Y, Cheng H, Ren C.
    Zhonghua Er Ke Za Zhi; 2015 Nov 11; 53(11):855-9. PubMed ID: 26758326
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  • 16. [Value of muscle studies in the early diagnosis of Schwartz-Jampel syndrome].
    Vanlieferighen P, Francannet C, Dechelotte P, Malpuech G, de Laguillaumie B, Storme B.
    J Genet Hum; 1987 Aug 11; 35(4):243-9. PubMed ID: 3655749
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  • 17. [Clinical analysis of four patients with Schwartz-Jampel syndrome].
    Zhang S, Wu HS, Lü JL.
    Zhonghua Er Ke Za Zhi; 2012 Mar 11; 50(3):231-4. PubMed ID: 22801212
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