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 *

307 related articles for article (PubMed ID: 17903057)

  • 21. Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues.
    Wang CH; Carter TA; Das K; Xu J; Ross BM; Penchaszadeh GK; Gilliam TC
    Ann Neurol; 1997 Jul; 42(1):41-9. PubMed ID: 9225684
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Sequence of a 131-kb region of 5q13.1 containing the spinal muscular atrophy candidate genes SMN and NAIP.
    Chen Q; Baird SD; Mahadevan M; Besner-Johnston A; Farahani R; Xuan J; Kang X; Lefebvre C; Ikeda JE; Korneluk RG; MacKenzie AE
    Genomics; 1998 Feb; 48(1):121-7. PubMed ID: 9503025
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy.
    Taylor JE; Thomas NH; Lewis CM; Abbs SJ; Rodrigues NR; Davies KE; Mathew CG
    Eur J Hum Genet; 1998; 6(5):467-74. PubMed ID: 9801871
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Spinal muscular atrophy due to double gene conversion event.
    Maamouri W; Hammer MB; Bouhlel Y; Souilem S; Khmiri N; Nehdi H; Hentati F; Amouri R
    Int J Neurosci; 2011 Feb; 121(2):107-11. PubMed ID: 21047176
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis of spinal muscular atrophy in Turkish families.
    Erdem H; Dayangaç D; Pehlivan S; Topaloglu H
    Cent Eur J Public Health; 2001 Feb; 9(1):35-7. PubMed ID: 11243588
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Deletion analysis of Bulgarian SMA families.
    Jordanova A; Stoyanova V; Uzunova M; Litvinenko I; Kremensky I
    Hum Mutat; 1998; 12(1):33-8. PubMed ID: 9633817
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Analysis of deletional damage in SMN1, SMN2, and NAIP genes in patients with spinal muscular atrophy in the northwestern region of Russia].
    Glotov AS; Kiselev AV; Ivashchenko TE; Baranov VS
    Genetika; 2001 Aug; 37(8):1156-9. PubMed ID: 11642117
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Analysis of the survival motor neuron and neuronal apoptosis inhibitory protein genes in Malay patients with Spinal Muscular Atrophy.
    Zilfalil BA; Zabidi-Hussin AM; Watihayati MS; Rozainah MY; Naing L; Sutomo R; Nishio H; Narazah MY; Matsuo M
    Med J Malaysia; 2004 Oct; 59(4):512-4. PubMed ID: 15779584
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Molecular basis of spinal muscular atrophy: th SMN gene].
    Tizzano E; Baiget M
    Neurologia; 2000 Nov; 15(9):393-400. PubMed ID: 11195146
    [TBL] [Abstract][Full Text] [Related]  

  • 30. SMA type 2 unrelated to chromosome 5q13.
    Nevo Y; Kramer U; Legum C; Shomrat R; Fatal A; Soffer D; Harel S; Shapira Y
    Am J Med Genet; 1998 Jan; 75(2):193-5. PubMed ID: 9450884
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Spinal muscular atrophy: untangling the knot?
    Biros I; Forrest S
    J Med Genet; 1999 Jan; 36(1):1-8. PubMed ID: 9950358
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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; 40(3):433-7. PubMed ID: 10411975
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Survival motor neuron gene and neuronal apoptosis inhibitory protein gene deletion in patients with spinal muscular atrophy].
    Ma S; Yuan L; Liu T; Yang T; Zhou W; Wu H
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2000 Dec; 22(6):551-4. PubMed ID: 12903402
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical application of the molecular diagnosis of spinal muscular atrophy: deletions of neuronal apoptosis inhibitor protein and survival motor neuron genes.
    Somerville MJ; Hunter AG; Aubry HL; Korneluk RG; MacKenzie AE; Surh LC
    Am J Med Genet; 1997 Mar; 69(2):159-65. PubMed ID: 9056553
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Detection of SMN gene deletions in spinal muscular atrophy].
    Yang T; Yuan L; Liu T; Zhou W; Wu H; Zhao S; Shun L; Huo L; Ma S; Lin Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Apr; 15(2):95-7. PubMed ID: 9531649
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Spinal muscular atrophy: clinical spectrum and genetic mutations in Pakistani children.
    Ibrahim S; Moatter T; Saleem AF
    Neurol India; 2012; 60(3):294-8. PubMed ID: 22824686
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Analysis of survival motor neuron gene conversion in patients with spinal muscular atrophy].
    He SX; Ge XS; Qu YJ; Jin YW; Wang H; Bai JL; Song F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):606-11. PubMed ID: 22161088
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal tests.
    Botta A; Tacconelli A; Bagni I; Giardina E; Bonifazi E; Pietropolli A; Clementi M; Novelli G
    Neurology; 2005 Nov; 65(10):1631-5. PubMed ID: 16301493
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Point mutation analysis of SMN1 gene in patients with spinal muscular atrophy].
    QU YJ; DU J; LI EZ; YANG YL; ZOU LP; BAI JL; WANG H; JIN YW; SONG F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):121-6. PubMed ID: 21462119
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular prenatal diagnosis of autosomal recessive childhood spinal muscular atrophies (SMAs).
    Essawi ML; Al-Attribi GM; Gaber KR; El-Harouni AA
    Gene; 2012 Nov; 509(1):120-3. PubMed ID: 22921322
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.