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 *

185 related articles for article (PubMed ID: 7581364)

  • 1. Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAs.
    Wirth B; Hahnen E; Morgan K; DiDonato CJ; Dadze A; Rudnik-Schöneborn S; Simard LR; Zerres K; Burghes AH
    Hum Mol Genet; 1995 Aug; 4(8):1273-84. PubMed ID: 7581364
    [TBL] [Abstract][Full Text] [Related]  

  • 2. SMN(T) and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): genotype/phenotype correlations with disease severity.
    Simard LR; Rochette C; Semionov A; Morgan K; Vanasse M
    Am J Med Genet; 1997 Oct; 72(1):51-8. PubMed ID: 9295075
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Genotype-phenotype correlation of SMN locus genes in spinal muscular atrophy patients from India.
    Kesari A; Idris MM; Chandak GR; Mittal B
    Exp Mol Med; 2005 Jun; 37(3):147-54. PubMed ID: 16000867
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counseling.
    Wirth B; Schmidt T; Hahnen E; Rudnik-Schöneborn S; Krawczak M; Müller-Myhsok B; Schönling J; Zerres K
    Am J Hum Genet; 1997 Nov; 61(5):1102-11. PubMed ID: 9345102
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular analysis of the SMN and NAIP genes in Spanish spinal muscular atrophy (SMA) families and correlation between number of copies of cBCD541 and SMA phenotype.
    Velasco E; Valero C; Valero A; Moreno F; Hernández-Chico C
    Hum Mol Genet; 1996 Feb; 5(2):257-63. PubMed ID: 8824882
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy.
    DiDonato CJ; Morgan K; Carpten JD; Fuerst P; Ingraham SE; Prescott G; McPherson JD; Wirth B; Zerres K; Hurko O
    Am J Hum Genet; 1994 Dec; 55(6):1218-29. PubMed ID: 7977383
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Correlation between genotype and phenotype in Korean patients with spinal muscular atrophy.
    Cho K; Ryu K; Lee E; Won S; Kim J; Yoo OJ; Hahn S
    Mol Cells; 2001 Feb; 11(1):21-7. PubMed ID: 11266116
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterisation of SMN hybrid genes in Spanish SMA patients: de novo, homozygous and compound heterozygous cases.
    Cuscó I; Barceló MJ; del Rio E; Martín Y; Hernández-Chico C; Bussaglia E; Baiget M; Tizzano EF
    Hum Genet; 2001 Mar; 108(3):222-9. PubMed ID: 11354634
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy.
    Wang CH; Xu J; Carter TA; Ross BM; Dominski MK; Bellcross CA; Penchaszadeh GK; Munsat TL; Gilliam TC
    Hum Mol Genet; 1996 Mar; 5(3):359-65. PubMed ID: 8852661
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Screening of deletions in SMN, NAIP and BTF2p44 genes in Turkish spinal muscular atrophy patients.
    Savas S; Gokgoz N; Kayserili H; Ozkinay F; Yuksel-Apak M; Kirdar B
    Hum Hered; 2000; 50(3):162-5. PubMed ID: 10686493
    [TBL] [Abstract][Full Text] [Related]  

  • 14. FISH detection of chromosome polymorphism and deletions in the spinal muscular atrophy (SMA) region of 5q13.
    Rajcan-Separovic E; Mahadevan MS; Lefebvre C; Besner-Johnston A; Ikeda JE; Korneluk RG; MacKenzie A
    Cytogenet Cell Genet; 1996; 75(4):243-7. PubMed ID: 9067434
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Deletion analysis of the simple tandem repeat loci physically linked to the spinal muscular atrophy locus.
    Capon F; Levato C; Bussaglia E; Lo Cicero S; Tizzano EF; Baiget M; Silani V; Pizzuti A; Novelli G; Dallapiccola B
    Hum Mutat; 1996; 7(3):198-201. PubMed ID: 8829652
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. De novo and inherited deletions of the 5q13 region in spinal muscular atrophies.
    Melki J; Lefebvre S; Burglen L; Burlet P; Clermont O; Millasseau P; Reboullet S; Bénichou B; Zeviani M; Le Paslier D
    Science; 1994 Jun; 264(5164):1474-7. PubMed ID: 7910982
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lower incidence of deletions in the survival of motor neuron gene and the neuronal apoptosis inhibitory protein gene in children with spinal muscular atrophy from Serbia.
    Miskovic M; Lalic T; Radivojevic D; Cirkovic S; Vlahovic G; Zamurovic D; Guc-Scekic M
    Tohoku J Exp Med; 2011 Nov; 225(3):153-9. PubMed ID: 21971302
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.