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Journal Abstract Search

96 related items for PubMed ID: 6502650

  • 1. Genetic heterogeneity in the Freeman-Sheldon syndrome: two adults with probable autosomal recessive inheritance.
    Fitzsimmons JS, Zaldua V, Chrispin AR.
    J Med Genet; 1984 Oct; 21(5):364-8. PubMed ID: 6502650
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  • 2. New evidence for genetic heterogeneity of the Freeman-Sheldon syndrome.
    Sánchez JM, Kaminker CP.
    Am J Med Genet; 1986 Nov; 25(3):507-11. PubMed ID: 3789012
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  • 4. Clinical analysis of a variant of Freeman-Sheldon syndrome (DA2B).
    Krakowiak PA, Bohnsack JF, Carey JC, Bamshad M.
    Am J Med Genet; 1998 Feb 26; 76(1):93-8. PubMed ID: 9508073
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  • 5. Distal arthrogryposis type IIB in a girl: autosomal recessive inheritance?
    Tsukahara M, Kajii T.
    Jinrui Idengaku Zasshi; 1984 Dec 26; 29(4):447-51. PubMed ID: 6535857
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  • 6. Autosomal-dominant inheritance of distal arthrogryposis.
    McCormack MK, Coppola-McCormack PJ, Lee ML.
    Am J Med Genet; 1980 Dec 26; 6(2):163-9. PubMed ID: 7446562
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  • 7. Arthrogryposis multiplex congenita: neurogenic type with autosomal recessive inheritance.
    Rosenmann A, Arad I.
    J Med Genet; 1974 Mar 26; 11(1):91-4. PubMed ID: 4837288
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  • 8. Prenatal growth retardation, pelvic hypoplasia, and arthrogrypotic changes of lower limbs: a distinct autosomal-recessive disorder.
    Sarralde A, Reynoso MC, Nazará Z, Soto F, Hernández A.
    Am J Med Genet; 1998 Feb 17; 75(5):453-60. PubMed ID: 9489787
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  • 9. Dominant distal arthrogryposis in a Maori family with marked variability of expression.
    Klemp P, Hall JG.
    Am J Med Genet; 1995 Feb 13; 55(4):414-9. PubMed ID: 7762579
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  • 11. The distal arthrogryposes: delineation of new entities--review and nosologic discussion.
    Hall JG, Reed SD, Greene G.
    Am J Med Genet; 1982 Feb 13; 11(2):185-239. PubMed ID: 7039311
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  • 14. A further heterogeneous locus contained in 8q21 for Freeman-Sheldon syndrome may be suggested by Kristin Hofmann.
    Li X, Jiang M, Han W.
    Eur J Med Genet; 2013 May 13; 56(5):278. PubMed ID: 23486078
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  • 16. Familial distal arthrogryposis type I.
    Stoll C, Alembik Y, Dott B.
    Ann Genet; 1996 May 13; 39(2):75-80. PubMed ID: 8766137
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  • 17. Familial arthrogryposis with distal involvement of the limbs.
    Kasai T, Oki T, Osuga T, Nogami H.
    Clin Orthop Relat Res; 1982 Jun 13; (166):182-4. PubMed ID: 7083669
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  • 18. Freeman-Sheldon syndrome: a disorder of congenital myopathic origin?
    Vanĕk J, Janda J, Amblerová V, Losan F.
    J Med Genet; 1986 Jun 13; 23(3):231-6. PubMed ID: 3723551
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  • 19. Arthrogryposis, perthes disease, and upward gaze palsy: a novel autosomal recessive syndromic form of arthrogryposis.
    Alkuraya FS.
    Am J Med Genet A; 2011 Feb 13; 155A(2):297-300. PubMed ID: 21271645
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