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Journal Abstract Search

70 related items for PubMed ID: 895985

  • 1. [Spinal muscle atrophy in the offspring of consanguineous parents].
    Borkowska J, Hausmanowa-Petrusewicz I.
    Neurol Neurochir Pol; 1977; 11(4):487-90. PubMed ID: 895985
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  • 2. The genetic heterogeneity of spinal muscular atrophy (SMA).
    Zellweger H.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):82-9. PubMed ID: 5173130
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  • 5. [Clinical picture, pathogenesis and geneology of hereditary progressive spinal muscular atrophies].
    Nesterov LN, Sushcheva GP, Viatkina SIa, Novikova NP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984 Feb; 84(3):321-30. PubMed ID: 6326437
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  • 6. The infantile proximal spinal muscular atrophies in Switzerland.
    Zellweger H, Hanhart E.
    Helv Paediatr Acta; 1972 Sep; 27(4):355-60. PubMed ID: 4644272
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  • 7. Consanguinity and deafness in Omani children.
    Khabori MA, Patton MA.
    Int J Audiol; 2008 Jan; 47(1):30-3. PubMed ID: 18196484
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  • 8. Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study.
    Teeuw ME, Henneman L, Bochdanovits Z, Heutink P, Kuik DJ, Cornel MC, Ten Kate LP.
    BMC Med Genet; 2010 Jul 16; 11():113. PubMed ID: 20637082
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  • 10. International collaborative study of the spinal muscular atrophies. Part 2. Analysis of genetic data.
    Emery AE, Davie AM, Holloway S, skinner R.
    J Neurol Sci; 1976 Dec 16; 30(2-3):375-84. PubMed ID: 1003252
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  • 11. Arthrogryposis multiplex congenita: neurogenic type with autosomal recessive inheritance.
    Rosenmann A, Arad I.
    J Med Genet; 1974 Mar 16; 11(1):91-4. PubMed ID: 4837288
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  • 12. Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.
    Temtamy SA, Shoukry AS, Raafat M, Mihareb S.
    Birth Defects Orig Artic Ser; 1975 Mar 16; 11(2):104-8. PubMed ID: 1227520
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  • 13. Recessive inheritance in a neuronal motor neuropathy form of peroneal muscular atrophy.
    Frajman M, Brilla E, Gutiérrez A, Hun L.
    Rev Invest Clin; 1983 Mar 16; 35(4):305-8. PubMed ID: 6672928
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  • 14. Autosomal dominant inheritance of hereditary canine spinal muscular atrophy.
    Sack GH, Cork LC, Morris JM, Griffin JW, Price DL.
    Ann Neurol; 1984 Apr 16; 15(4):369-73. PubMed ID: 6742782
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  • 16. Late-childhood-onset spinal muscular atrophy in three Melanesian families in Papua New guinea.
    Scrimgeour EM, Mastaglia FL.
    Am J Med Genet; 1984 Dec 16; 19(4):769-77. PubMed ID: 6517100
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  • 18. Evidence for autosomal recessive inheritance of infantile dilated cardiomyopathy: studies from the Eastern Province of Saudi Arabia.
    Seliem MA, Mansara KB, Palileo M, Ye X, Zhang Z, Benson DW.
    Pediatr Res; 2000 Dec 16; 48(6):770-5. PubMed ID: 11102545
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  • 19. Cluster of acute infantile spinal muscular atrophy (Werdnig-Hoffmann disease) in a limited area of Reunion Island.
    Pascalet-Guidon MJ, Bois E, Feingold J, Mattei JF, Combes JC, Hamon C.
    Clin Genet; 1984 Jul 16; 26(1):39-42. PubMed ID: 6467653
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  • 20. Chylous ascites in sibs from a consanguineous marriage.
    Flores S, Leungas J, Arredondo-Vega F, Guízar-Vázquez J.
    Am J Med Genet; 1979 Jul 16; 3(2):145-8. PubMed ID: 474627
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