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Journal Abstract Search

138 related items for PubMed ID: 4837288

  • 21. Arthrogryposis multiplex congenita: histochemical study of biopsied muscles.
    Uchida T, Nonaka I, Yokochi K, Kodama K.
    Pediatr Neurol; 1985; 1(3):169-73. PubMed ID: 3880402
    [Abstract] [Full Text] [Related]

  • 22. Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita.
    Ekhilevitch N, Kurolap A, Oz-Levi D, Mory A, Hershkovitz T, Ast G, Mandel H, Baris HN.
    Clin Genet; 2016 Jul; 90(1):84-9. PubMed ID: 26661508
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  • 23. Linkage mapping of the locus for inherited ovine arthrogryposis (IOA) to sheep chromosome 5.
    Murphy AM, MacHugh DE, Park SD, Scraggs E, Haley CS, Lynn DJ, Boland MP, Doherty ML.
    Mamm Genome; 2007 Jan; 18(1):43-52. PubMed ID: 17242863
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  • 24. Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system.
    Illum N, Reske-Nielsen E, Skovby F, Askjaer SA, Bernsen A.
    Neuropediatrics; 1988 Nov; 19(4):186-92. PubMed ID: 3205375
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  • 25. Distal arthrogryposis type IIB in a girl: autosomal recessive inheritance?
    Tsukahara M, Kajii T.
    Jinrui Idengaku Zasshi; 1984 Dec; 29(4):447-51. PubMed ID: 6535857
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  • 27. A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.
    Shohat M, Lotan R, Magal N, Shohat T, Fischel-Ghodsian N, Rotter JI, Jaber L.
    Am J Hum Genet; 1997 Nov; 61(5):1139-43. PubMed ID: 9345093
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  • 30. Arthrogryposis multiplex with deafness, inguinal hernias, and early death: a family report of a probably autosomal recessive trait.
    Tiemann C, Bührer C, Burwinkel B, Wirtenberger M, Hoehn T, Hübner C, van Landeghem FK, Stoltenburg G, Obladen M.
    Am J Med Genet A; 2005 Aug 30; 137(2):125-9. PubMed ID: 16059941
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  • 33. Genetics of arthrogryposis: linkage analysis approach.
    Narkis G, Landau D, Manor E, Ofir R, Birk OS.
    Clin Orthop Relat Res; 2007 Mar 30; 456():30-5. PubMed ID: 17195815
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  • 34. The neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis.
    Dieterich K, Quijano-Roy S, Monnier N, Zhou J, Fauré J, Smirnow DA, Carlier R, Laroche C, Marcorelles P, Mercier S, Mégarbané A, Odent S, Romero N, Sternberg D, Marty I, Estournet B, Jouk PS, Melki J, Lunardi J.
    Hum Mol Genet; 2013 Apr 15; 22(8):1483-92. PubMed ID: 23236030
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  • 37. Arthrogryposis multiplex congenita: an autopsy case of a fatal form.
    Imamura M, Yamanaka N, Nakamura F, Oyanagi K.
    Hum Pathol; 1981 Aug 15; 12(8):699-704. PubMed ID: 7286967
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  • 39. Restrictive dermopathy: a report of three cases.
    Mok Q, Curley R, Tolmie JL, Marsden RA, Patton MA, Davies EG.
    J Med Genet; 1990 May 15; 27(5):315-9. PubMed ID: 2352259
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