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Journal Abstract Search

173 related items for PubMed ID: 8152204

  • 1. [Indirect molecular-genetic family study and prenatal diagnosis of infantile spinal muscular atrophy].
    Heber U, Müller CR.
    Klin Padiatr; 1994; 206(1):30-5. PubMed ID: 8152204
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of Werdnig-Hoffmann disease: DNA analysis of a mummified umbilical cord using closely linked microsatellite markers.
    Matilla T, Corral J, Miranda M, Troyano J, Morrison K, Volpini V, Estivill X.
    Prenat Diagn; 1994 Mar; 14(3):219-22. PubMed ID: 8052572
    [Abstract] [Full Text] [Related]

  • 3. A recombination event occurring within two complex 5q13.1 microsatellite repeat polymorphisms suggests a telomeric mapping of spinal muscular atrophy.
    Yaraghi Z, McLean MD, Roy N, Surh L, Ikeda JE, Korneluk RG, MacKenzie A.
    Hum Genet; 1995 Sep; 96(3):330-4. PubMed ID: 7649551
    [Abstract] [Full Text] [Related]

  • 4. Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA).
    Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Grewal PK, Dennis C, Buckle V, Ignatius J, Dubowitz V.
    Hum Genet; 1993 Sep; 92(2):133-8. PubMed ID: 8370578
    [Abstract] [Full Text] [Related]

  • 5. Confirmation of clinical diagnosis in requests for prenatal prediction of SMA type I.
    Cobben JM, de Visser M, Scheffer H, Osinga J, van der Steege G, Buys CH, van Ommen GJ, ten Kate LP.
    J Neurol Neurosurg Psychiatry; 1993 Mar; 56(3):319-21. PubMed ID: 8459253
    [Abstract] [Full Text] [Related]

  • 6. Rapid diagnosis of infantile spinal muscular atrophy by direct amplification of amniocyte and CVS DNA.
    MacKenzie A, Besner A, Roy N.
    J Med Genet; 1993 Feb; 30(2):162-3. PubMed ID: 8445624
    [No Abstract] [Full Text] [Related]

  • 7. [The gene of spinal muscular atrophy localized. Possibilities for prenatal diagnosis].
    Blennow ES, Bui TH, Söderhäll S, Anvret M, Nordenskjöld M.
    Lakartidningen; 1993 Jan 27; 90(4):269-75. PubMed ID: 8433608
    [No Abstract] [Full Text] [Related]

  • 8. Prenatal prediction of spinal muscular atrophy.
    Daniels RJ, Suthers GK, Morrison KE, Thomas NH, Francis MJ, Mathew CG, Loughlin S, Heiberg A, Wood D, Dubowitz V.
    J Med Genet; 1992 Mar 27; 29(3):165-70. PubMed ID: 1348091
    [Abstract] [Full Text] [Related]

  • 9. High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5.
    Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Buckle VJ, Davies KE.
    Am J Hum Genet; 1992 Mar 27; 50(3):520-7. PubMed ID: 1539593
    [Abstract] [Full Text] [Related]

  • 10. Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system.
    Shaw SW, Cheng PJ, Chang SD, Lin YT, Hung CC, Chen CP, Su YN.
    Acta Obstet Gynecol Scand; 2008 Mar 27; 87(9):960-8. PubMed ID: 18720039
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of the acute form of proximal spinal muscular atrophy: experience on the acceptance of linkage analyses by the families.
    Huschenbett J, Hanke R, Pfeifer L, Speer A.
    Prenat Diagn; 1993 Jul 27; 13(7):643-9. PubMed ID: 8105458
    [Abstract] [Full Text] [Related]

  • 12. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.
    Gilliam TC, Brzustowicz LM, Castilla LH, Lehner T, Penchaszadeh GK, Daniels RJ, Byth BC, Knowles J, Hislop JE, Shapira Y.
    Nature; 1990 Jun 28; 345(6278):823-5. PubMed ID: 1972783
    [Abstract] [Full Text] [Related]

  • 13. Spinal muscular atrophy in childhood.
    Fidziańska A.
    Semin Pediatr Neurol; 1996 Jun 28; 3(2):53-8. PubMed ID: 8795842
    [Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of Werdnig-Hoffmann disease in China.
    Feng J, Toshiyuki Y.
    Chin Med J (Engl); 2003 May 28; 116(5):673-5. PubMed ID: 12875676
    [Abstract] [Full Text] [Related]

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  • 17. [Spinal muscular atrophy in childhood. Possibilities and limits of clinical and molecular genetic diagnosis].
    Zerres K, Rudnik-Schöneborn S, Röhrig D, Wirth B.
    Monatsschr Kinderheilkd; 1993 Nov 28; 141(11):848-54. PubMed ID: 8283989
    [Abstract] [Full Text] [Related]

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  • 19. Two 5q13 simple tandem repeat loci are in linkage disequilibrium with type 1 spinal muscular atrophy.
    McLean MD, Roy N, MacKenzie AE, Salih M, Burghes AH, Simard L, Korneluk RG, Ikeda JE, Surh L.
    Hum Mol Genet; 1994 Nov 28; 3(11):1951-6. PubMed ID: 7874111
    [Abstract] [Full Text] [Related]

  • 20. Spinal muscular atrophies.
    Lancet; 1990 Aug 04; 336(8710):280-1. PubMed ID: 1973974
    [No Abstract] [Full Text] [Related]

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