These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 8052572)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 50(3):520-7. PubMed ID: 1539593
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Genetic linkage analysis of Canadian spinal muscular atrophy kindreds using flanking microsatellite 5q13 polymorphisms.
    MacKenzie A; Roy N; Besner A; Mettler G; Jacob P; Korneluk R; Surh L
    Hum Genet; 1993 Jan; 90(5):501-4. PubMed ID: 8094064
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 29(3):165-70. PubMed ID: 1348091
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6.
    Brzustowicz LM; Kleyn PW; Boyce FM; Lien LL; Monaco AP; Penchaszadeh GK; Das K; Wang CH; Munsat TL; Ott J
    Genomics; 1992 Aug; 13(4):991-8. PubMed ID: 1505990
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 13(7):643-9. PubMed ID: 8105458
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3.
    Wirth B; Pick E; Leutner A; Dadze A; Voosen B; Knapp M; Piechaczek-Wappenschmidt B; Rudnik-Schöneborn S; Schönling J; Cox S
    Genomics; 1994 Mar; 20(1):84-93. PubMed ID: 7912691
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. First-trimester prenatal diagnosis of spinal muscular atrophy using microsatellite markers.
    Lo Cicero S; Capon F; Melchionda S; Gennarelli M; Novelli G; Dallapiccola B
    Prenat Diagn; 1994 Jun; 14(6):459-62. PubMed ID: 7937582
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.
    Melki J; Abdelhak S; Burlet P; Raclin V; Kaplan J; Spiegel R; Gilgenkrantz S; Philip N; Chauvet ML; Dumez Y
    J Med Genet; 1992 Mar; 29(3):171-4. PubMed ID: 1348092
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Isolation of microsatellites from the spinal muscular atrophy (SMA) candidate region on chromosome 5q and linkage analysis in Spanish SMA families.
    Velasco E; Valero C; García E; de la Puente A; Cruces J; San Millán JL; del Castillo I; Coloma A; Moreno F; Hernández-Chico C
    Eur J Hum Genet; 1995; 3(2):96-101. PubMed ID: 7552147
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Microsatellite polymorphisms for chromosome 5 bands q11.2-q13.3.
    Sherrington R; Mankoo B; Dixon M; Curtis D; Kalsi G; Melmer G; Gurling H
    Hum Hered; 1993; 43(3):197-202. PubMed ID: 8330884
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.
    Brzustowicz LM; Mérette C; Kleyn PW; Lehner T; Castilla LH; Penchaszadeh GK; Das K; Munsat TL; Ott J; Gilliam TC
    Hum Hered; 1993; 43(6):380-7. PubMed ID: 7904586
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. Linkage and apparent heterogeneity in proximal spinal muscular atrophies.
    Cobben JM; Scheffer H; De Visser M; Osinga J; Frants R; van der Steege G; Wijmenga C; ten Kate LP; van Ommen GJ; Buys CH
    Neuromuscul Disord; 1993 Jul; 3(4):327-33. PubMed ID: 8268730
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.