BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 1857931)

  • 1. [Localization of the spinal muscular atrophy gene by reverse genetic methods. Prospect of a gene on chromosome 5].
    Melki J
    Rev Prat; 1991 Jun; 41(18):1677-9. PubMed ID: 1857931
    [No Abstract]   [Full Text] [Related]  

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

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

  • 4. Prenatal onset spinal muscular atrophy.
    MacLeod MJ; Taylor JE; Lunt PW; Mathew CG; Robb SA
    Eur J Paediatr Neurol; 1999; 3(2):65-72. PubMed ID: 10700541
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and molecular diagnosis of spinal muscular atrophy.
    Panigrahi I; Kesari A; Phadke SR; Mittal B
    Neurol India; 2002 Jun; 50(2):117-22. PubMed ID: 12134171
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis for risk of spinal muscular atrophy.
    Cuscó I; Barceló MJ; Soler C; Parra J; Baiget M; Tizzano E
    BJOG; 2002 Nov; 109(11):1244-9. PubMed ID: 12452462
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Genetic diagnosis of the hypotonic newborn].
    Bauer MS
    Rev Neurol; 1997 May; 25(141):703-6. PubMed ID: 9206594
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Preserved umbilical cord facilitates antenatal diagnosis of spinal muscular atrophy.
    Kabra M; Arora S; Maria A; Aggarwal R
    Indian Pediatr; 2003 May; 40(5):415-8. PubMed ID: 12768044
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spinal muscular atrophy of childhood: genetics.
    Raymond FL
    Dev Med Child Neurol; 1997 Jun; 39(6):419-20. PubMed ID: 9233369
    [No Abstract]   [Full Text] [Related]  

  • 10. [Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies].
    Melki J; Lefebvre S; Burglen L; Burlet P; Clermont O; Millasseau P; Reboulet S; Benichou B; Zeviani M; Le Paslier D
    C R Seances Soc Biol Fil; 1994; 188(5-6):495-8. PubMed ID: 7780792
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy].
    Spiegel R; Hagmann A; Boltshauser E; Moser H
    Schweiz Med Wochenschr; 1996 May; 126(21):907-14. PubMed ID: 8693311
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Werdnig-Hoffmann disease. The first prenatal diagnosis in Cuba].
    Acevedo-López AM; Zaldívar-Vaillant T; Hernández-Chico C; Moreno F; Rosich-Capablanca G; Guerra-Badía R
    Rev Neurol; 1999 Dec 16-31; 29(12):1172-5. PubMed ID: 10652743
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Spinal muscular atrophy (type I, II)].
    Saito K; Shishikura K; Suzuki H; Osawa M
    Ryoikibetsu Shokogun Shirizu; 1999; (27 Pt 2):364-70. PubMed ID: 10434675
    [No Abstract]   [Full Text] [Related]  

  • 14. Programmed cell death and the gene behind spinal muscular atrophy.
    Robinson A
    CMAJ; 1995 Nov; 153(10):1459-62. PubMed ID: 7585374
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 87(9):960-8. PubMed ID: 18720039
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of spinal muscular atrophy in Chinese by genetic analysis of fetal cells.
    Wu T; Ding XS; Li WL; Yao J; Deng XX
    Chin Med J (Engl); 2005 Aug; 118(15):1274-7. PubMed ID: 16117881
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and molecular genetic features of congenital spinal muscular atrophy.
    Devriendt K; Lammens M; Schollen E; Van Hole C; Dom R; Devlieger H; Cassiman JJ; Fryns JP; Matthijs G
    Ann Neurol; 1996 Nov; 40(5):731-8. PubMed ID: 8957014
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 345(6278):823-5. PubMed ID: 1972783
    [TBL] [Abstract][Full Text] [Related]  

  • 19. What is the value for money of prenatal carrier screening for spinal muscular atrophy? Too soon to say.
    Grosse SD
    Am J Obstet Gynecol; 2010 Mar; 202(3):209-11. PubMed ID: 20207235
    [No Abstract]   [Full Text] [Related]  

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

    [Next]    [New Search]
    of 6.