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Journal Abstract Search

203 related items for PubMed ID: 7137221

  • 1. 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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  • 2. [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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  • 3. Autosomal recessive Robinow syndrome.
    Teebi AS.
    Am J Med Genet; 1990 Jan; 35(1):64-8. PubMed ID: 2301471
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  • 4. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
    Chitayat D, Hall JG, Couch RM, Phang MS, Baldwin VJ.
    Am J Med Genet; 1990 Sep; 37(1):65-70. PubMed ID: 2240046
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  • 6. Schwartz-Jampel syndrome: three pediatric case reports.
    Yapicioğlu H, Satar M, Yildizdaş D, Narli N, Suleymanova D, Tutak E.
    Genet Couns; 2003 Sep; 14(3):353-8. PubMed ID: 14577682
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  • 12. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
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  • 14. Pitt-Rogers-Danks syndrome: further delineation.
    Lizcano-Gil LA, García-Cruz D, García-Cruz O, Sánchez-Corona J.
    Am J Med Genet; 1995 Feb 13; 55(4):420-2. PubMed ID: 7762580
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  • 15. A child with sclerocornea, short limbs, short stature, and distinct facial appearance.
    Thompson EM, Winter RM.
    Am J Med Genet; 1988 Jul 13; 30(3):719-24. PubMed ID: 3055984
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  • 16. A case of Schwartz-Jampel syndrome with cleft palate.
    Abdel-Aziz M, Azab NA.
    Int J Pediatr Otorhinolaryngol; 2009 Nov 13; 73(11):1601-3. PubMed ID: 19733405
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  • 18. Schwartz-Jampel syndrome: I. Clinical, electromyographic, and histologic studies.
    Spaans F, Theunissen P, Reekers AD, Smit L, Veldman H.
    Muscle Nerve; 1990 Jun 13; 13(6):516-27. PubMed ID: 2366824
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  • 20. A new autosomal recessive disorder resembling Weaver syndrome.
    Teebi AS, Sundareshan TS, Hammouri MY, al-Awadi SA, al-Saleh QA.
    Am J Med Genet; 1989 Aug 13; 33(4):479-82. PubMed ID: 2596508
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