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.
2. Detection of homozygous and heterozygous SMN deletions of spinal muscular atrophy in a single assay with multiplex ligation-dependent probe amplification. Tomaszewicz K; Kang P; Wu BL Beijing Da Xue Xue Bao Yi Xue Ban; 2005 Feb; 37(1):55-7. PubMed ID: 15719043 [TBL] [Abstract][Full Text] [Related]
3. [A study of survival motor neuron and neuronal apoptosis inhibitory protein gene in spinal muscular atrophy]. Zhang L; Yang X; Xiao B Zhonghua Nei Ke Za Zhi; 2001 Jun; 40(6):401-4. PubMed ID: 11798607 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. [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]
6. [Diagnostic image (29). Adult form of proximal spinal muscular atrophy]. Bronner IM; Linssen WH; de Visser M Ned Tijdschr Geneeskd; 2001 Mar; 145(11):530. PubMed ID: 11284287 [TBL] [Abstract][Full Text] [Related]
13. Study of survival of motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) gene deletions in SMA patients. Kesari A; Misra UK; Kalita J; Mishra VN; Pradhan S; Patil SJ; Phadke SR; Mittal B J Neurol; 2005 Jun; 252(6):667-71. PubMed ID: 15772743 [TBL] [Abstract][Full Text] [Related]
14. Survival motor neuron protein regulates apoptosis in an in vitro model of spinal muscular atrophy. Parker GC; Li X; Anguelov RA; Toth G; Cristescu A; Acsadi G Neurotox Res; 2008 Jan; 13(1):39-48. PubMed ID: 18367439 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Adolescent spinal muscular atrophy with calf hypertrophy and a deletion in the SMN gene. Yiu EM; Ravat S; Ryan MM; Shield LK; Smith LJ; Kornberg AJ Muscle Nerve; 2008 Jul; 38(1):930-2. PubMed ID: 18508340 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy. Sun Y; Grimmler M; Schwarzer V; Schoenen F; Fischer U; Wirth B Hum Mutat; 2005 Jan; 25(1):64-71. PubMed ID: 15580564 [TBL] [Abstract][Full Text] [Related]
19. Therapeutics development for spinal muscular atrophy. Sumner CJ NeuroRx; 2006 Apr; 3(2):235-45. PubMed ID: 16554261 [TBL] [Abstract][Full Text] [Related]
20. Gene deletion patterns in spinal muscular atrophy patients with different clinical phenotypes. Haider MZ; Moosa A; Dalal H; Habib Y; Reynold L J Biomed Sci; 2001; 8(2):191-6. PubMed ID: 11287750 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]