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 *

653 related articles for article (PubMed ID: 8693311)

  • 1. [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]  

  • 2. Deletions in the SMN and NAIP genes in patients with spinal muscular atrophy in Croatia.
    Sertić J; Barisić N; Sostarko M; Bosnjak N; Culić V; Cvitanović L; Ferencak G; Brzović Z; Stavljenić-Rukavina A
    Coll Antropol; 1997 Dec; 21(2):487-92. PubMed ID: 9439064
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy.
    Al-Jumah M; Majumdar R; Al-Rajeh S; Awada A; Chaves-Carbello E; Salih M; Al-Shahwan S; Al-Subiey K; Al-Uthaim S
    Saudi Med J; 2003 Oct; 24(10):1052-4. PubMed ID: 14578966
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. NAIP-deletion analysis in Malaysian patients with spinal muscular atrophy.
    Watihayati MS; Zabidi AM; Tang TH; Nishio H; Zilfalil BA
    Kobe J Med Sci; 2007; 53(4):171-5. PubMed ID: 17932457
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy.
    Watihayati MS; Fatemeh H; Marini M; Atif AB; Zahiruddin WM; Sasongko TH; Tang TH; Zabidi-Hussin ZA; Nishio H; Zilfalil BA
    Brain Dev; 2009 Jan; 31(1):42-5. PubMed ID: 18842367
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings.
    Rudnik-Schöneborn S; Forkert R; Hahnen E; Wirth B; Zerres K
    Neuropediatrics; 1996 Feb; 27(1):8-15. PubMed ID: 8677029
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients.
    Bouhouche A; Benomar A; Birouk N; Bouslam N; Ouazzani R; Yahyaoui M; Chkili T
    J Neurol; 2003 Oct; 250(10):1209-13. PubMed ID: 14586604
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals.
    Hahnen E; Forkert R; Marke C; Rudnik-Schöneborn S; Schönling J; Zerres K; Wirth B
    Hum Mol Genet; 1995 Oct; 4(10):1927-33. PubMed ID: 8595417
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Diagnostic progress in spinal muscular atrophy].
    Gergont A; Kaciński M; Steczkowska-Klucznik M
    Przegl Lek; 2001; 58(11):989-91. PubMed ID: 11987841
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. 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]  

  • 13. 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]  

  • 14. [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]  

  • 15. Molecular genetics of spinal muscular atrophy: contribution of the NAIP gene to clinical severity.
    Akutsu T; Nishio H; Sumino K; Takeshima Y; Tsuneishi S; Wada H; Takada S; Matsuo M; Nakamura H
    Kobe J Med Sci; 2002 Apr; 48(1-2):25-31. PubMed ID: 11912351
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spinal Muscular Atrophies: An Ongoing Diagnostic Dilemma?
    Biros I; Forshaw K; Sheffield LJ; Kornberg AJ; Forrest S
    Mol Diagn; 1997 Dec; 2(4):241-249. PubMed ID: 10462616
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease.
    Burlet P; Bürglen L; Clermont O; Lefebvre S; Viollet L; Munnich A; Melki J
    J Med Genet; 1996 Apr; 33(4):281-3. PubMed ID: 8730281
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3.
    Brzustowicz LM; Lehner T; Castilla LH; Penchaszadeh GK; Wilhelmsen KC; Daniels R; Davies KE; Leppert M; Ziter F; Wood D
    Nature; 1990 Apr; 344(6266):540-1. PubMed ID: 2320125
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. 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; 344(6268):767-8. PubMed ID: 1970420
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 33.