225 related articles for article (PubMed ID: 21338334)
1. Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy.
Sasongko TH; Gunadi ; Zilfalil BA; Zabidi-Hussin Z
J Neurogenet; 2011 Mar; 25(1-2):15-6. PubMed ID: 21338334
[TBL] [Abstract][Full Text] [Related]
2. [Gene diagnosis for spinal muscular atrophy and its application study].
Cao DH; Ren MH; Lin CK; Cui WT; Ma HW; Wu YY; Jin CL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):306-9. PubMed ID: 19504445
[TBL] [Abstract][Full Text] [Related]
3. [Quantitative analysis of the genes determining spinal muscular atrophy].
Nagymihály M; Herczegfalvi A; Tímár L; Karcagi V
Ideggyogy Sz; 2009 Nov; 62(11-12):390-7. PubMed ID: 20025129
[TBL] [Abstract][Full Text] [Related]
4. [Study of SMN gene in Chinese children with spinal muscular atrophy].
Liu WL; Li F; Ma HW; Li HY
Zhongguo Dang Dai Er Ke Za Zhi; 2010 Jul; 12(7):539-43. PubMed ID: 20637152
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [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]
7. [Mutation analysis of SMN gene in a patient and his family with spinal muscular atrophy].
Zeng J; Lin YH; Yan AZ; Cai MY; Ke LF; Lan FH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):139-43. PubMed ID: 19350502
[TBL] [Abstract][Full Text] [Related]
8. Rapid diagnosis of spinal muscular atrophy using tetra-primer ARMS PCR assay: simultaneous detection of SMN1 and SMN2 deletion.
Baris I; Etlik O; Koksal V; Arican-Baris ST
Mol Cell Probes; 2010 Jun; 24(3):138-41. PubMed ID: 20025960
[TBL] [Abstract][Full Text] [Related]
9. High-resolution melting (HRM) analysis as a feasible method for detecting spinal muscular atrophy via dried blood spots.
Er TK; Kan TM; Su YF; Liu TC; Chang JG; Hung SY; Jong YJ
Clin Chim Acta; 2012 Nov; 413(21-22):1781-5. PubMed ID: 22771969
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Molecular analysis of the SMN gene mutations in spinal muscular atrophy patients in China.
Liu WL; Li F; He ZX; Ai R; Ma HW
Genet Mol Res; 2013 Sep; 12(3):3598-604. PubMed ID: 24085424
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Rapid diagnosis of spinal muscular atrophy using denaturing high-performance liquid chromatography.
Chen WJ; Wu ZY; Wang N; Lin MT; Mu-Rong SX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):291-3. PubMed ID: 15952118
[TBL] [Abstract][Full Text] [Related]
14. Genetic testing and risk assessment for spinal muscular atrophy (SMA).
Ogino S; Wilson RB
Hum Genet; 2002 Dec; 111(6):477-500. PubMed ID: 12436240
[TBL] [Abstract][Full Text] [Related]
15. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA).
Wirth B
Hum Mutat; 2000; 15(3):228-37. PubMed ID: 10679938
[TBL] [Abstract][Full Text] [Related]
16. Multiplex ligation-dependent probe amplification improves diagnostics in spinal muscular atrophy.
Arkblad EL; Darin N; Berg K; Kimber E; Brandberg G; Lindberg C; Holmberg E; Tulinius M; Nordling M
Neuromuscul Disord; 2006 Dec; 16(12):830-8. PubMed ID: 17049859
[TBL] [Abstract][Full Text] [Related]
17. HnRNP C1/C2 may regulate exon 7 splicing in the spinal muscular atrophy gene SMN1.
Irimura S; Kitamura K; Kato N; Saiki K; Takeuchi A; Gunadi ; Matsuo M; Nishio H; Lee MJ
Kobe J Med Sci; 2009 Mar; 54(5):E227-36. PubMed ID: 19628962
[TBL] [Abstract][Full Text] [Related]
18. Compound heterozygous mutation in two unrelated cases of Chinese spinal muscular atrophy patients.
Qu YJ; Song F; Yang YL; Jin YW; Bai JL
Chin Med J (Engl); 2011 Feb; 124(3):385-9. PubMed ID: 21362338
[TBL] [Abstract][Full Text] [Related]
19. Multi-exon genotyping of SMN gene in spinal muscular atrophy by universal fluorescent PCR and capillary electrophoresis.
Wang CC; Chang JG; Chen YL; Jong YJ; Wu SM
Electrophoresis; 2010 Jul; 31(14):2396-404. PubMed ID: 20564270
[TBL] [Abstract][Full Text] [Related]
20. Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis.
Chen WJ; Wu ZY; Lin MT; Su JF; Lin Y; Murong SX; Wang N
Arch Neurol; 2007 Feb; 64(2):225-31. PubMed ID: 17296838
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
