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Journal Abstract Search

137 related items for PubMed ID: 1348092

  • 1.
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  • 2. 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
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  • 3. Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q.
    Melki J, Abdelhak S, Sheth P, Bachelot MF, Burlet P, Marcadet A, Aicardi J, Barois A, Carriere JP, Fardeau M.
    Nature; 1990 Apr 19; 344(6268):767-8. PubMed ID: 1970420
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  • 5. [Indirect molecular-genetic family study and prenatal diagnosis of infantile spinal muscular atrophy].
    Heber U, Müller CR.
    Klin Padiatr; 1994 Apr 19; 206(1):30-5. PubMed ID: 8152204
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  • 7. 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 19; 92(2):133-8. PubMed ID: 8370578
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  • 8. Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy Investigators.
    Melki J, Sheth P, Abdelhak S, Burlet P, Bachelot MF, Lathrop MG, Frezal J, Munnich A.
    Lancet; 1990 Aug 04; 336(8710):271-3. PubMed ID: 1973971
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  • 9. Prenatal diagnosis of spinal muscular atrophy type I (Werdnig- hoffmann) by DNA deletion analysis of cultivated amniocytes.
    Stipoljev F, Sertić J, Latin V, Rukavina-Stavljenić A, Kurjak A.
    Croat Med J; 1999 Sep 04; 40(3):433-7. PubMed ID: 10411975
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  • 10. 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
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  • 13. [Spinal muscular atrophy in young infants].
    Smit LM, Hageman EG.
    Tijdschr Kindergeneeskd; 1989 Jun 28; 57(3):102-6. PubMed ID: 2799798
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  • 14. 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 28; 13(7):643-9. PubMed ID: 8105458
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  • 15. Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele.
    Daniels RJ, Campbell L, Rodrigues NR, Francis MJ, Morrison KE, McLean M, MacKenzie A, Ignatius J, Dubowitz V, Davies KE.
    J Med Genet; 1995 Feb 28; 32(2):93-6. PubMed ID: 7760328
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  • 16. [Role of signs of fetal hypokinesia in the diagnosis of spinal muscular atrophy of neonatal onset].
    González De Dios J, Martínez Frías ML, Arroyo Carrera I, Fondevilla Saucí J, Sanchís Calvo A, Hernández Ramón F, Martínez Guardia N, García González MM.
    An Esp Pediatr; 2002 Mar 28; 56(3):233-40. PubMed ID: 11864521
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  • 20. [Cerebral agyria-pachygyria in a child with Werdnig-Hoffmann disease].
    Cneude F, Sukno S, Boidein F, Dehouck MB, Bourlet A, Vittu G.
    Rev Neurol (Paris); 1999 Sep 28; 155(8):589-91. PubMed ID: 10486849
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