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.
226 related articles for article (PubMed ID: 21055263)
1. [Genetic tests and clinical re-evaluation of 85 children with suspected spinal muscular atrophy]. Ji X; Liu XQ; Shen JW; Li XH; Tao J Zhonghua Er Ke Za Zhi; 2010 Jun; 48(6):425-30. PubMed ID: 21055263 [TBL] [Abstract][Full Text] [Related]
2. Correlation between deletion patterns of SMN and NAIP genes and the clinical features of spinal muscular atrophy in Indian patients. Dastur RS; Gaitonde PS; Khadilkar SV; Udani VP; Nadkarni JJ Neurol India; 2006 Sep; 54(3):255-9. PubMed ID: 16936383 [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. [Molecular analysis of survival motor neuron gene in 338 suspicious children patients with spinal muscular atrophy]. Song F; Qu YJ; Zou LP; Wang LW; Long MJ; Wang X; Yang YL; Chen Q; Wang H; Jin YW Zhonghua Er Ke Za Zhi; 2008 Dec; 46(12):919-23. PubMed ID: 19134255 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. [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]
8. 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]
9. Deletions in the survival motor neuron gene in Iranian patients with spinal muscular atrophy. Hasanzad M; Golkar Z; Kariminejad R; Hadavi V; Almadani N; Afroozan F; Salahshurifar I; Shafeghati Y; Kahrizi K; Najmabadi H Ann Acad Med Singap; 2009 Feb; 38(2):139-41. PubMed ID: 19271042 [TBL] [Abstract][Full Text] [Related]
10. Molecular analysis of the SMN1 and NAIP genes in Iranian patients with spinal muscular atrophy. Derakhshandeh-Peykar P; Esmaili M; Ousati-Ashtiani Z; Rahmani M; Babrzadeh F; Farshidi S; Attaran E; Sajedifar MM; Farhud DD Ann Acad Med Singap; 2007 Nov; 36(11):937-41. PubMed ID: 18071605 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Spinal muscular atrophy genetic testing experience at an academic medical center. Ogino S; Leonard DG; Rennert H; Wilson RB J Mol Diagn; 2002 Feb; 4(1):53-8. PubMed ID: 11826188 [TBL] [Abstract][Full Text] [Related]
13. Deletion analysis of SMN1 and NAIP genes in Southern Chinese children with spinal muscular atrophy. Liang YH; Chen XL; Yu ZS; Chen CY; Bi S; Mao LG; Zhou BL; Zhang XN J Zhejiang Univ Sci B; 2009 Jan; 10(1):29-34. PubMed ID: 19198020 [TBL] [Abstract][Full Text] [Related]
14. Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents. Chang JG; Jong YJ; Lin SP; Soong BW; Tsai CH; Yang TY; Chang CP; Wang WS Hum Genet; 1997 Oct; 100(5-6):577-81. PubMed ID: 9341874 [TBL] [Abstract][Full Text] [Related]
15. [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]
16. Preimplantation genetic diagnosis of spinal muscular atrophy. Dreesen JC; Bras M; de Die-Smulders C; Dumoulin JC; Cobben JM; Evers JL; Smeets HJ; Geraedts JP Mol Hum Reprod; 1998 Sep; 4(9):881-5. PubMed ID: 9783849 [TBL] [Abstract][Full Text] [Related]
17. [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]
19. Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene. Zarkov M; Stojadinović A; Sekulić S; Barjaktarović I; Perić S; Keković G; Drasković B; Stević Z Vojnosanit Pregl; 2015 Oct; 72(10):859-63. PubMed ID: 26665550 [TBL] [Abstract][Full Text] [Related]
20. [Mutation analysis of SMN1 gene in patients with spinal muscular atrophy]. DU J; Qu YJ; Xiong H; Li EZ; Jin YW; Bai JL; Wang H; Song F Zhonghua Er Ke Za Zhi; 2011 Jun; 49(6):411-5. PubMed ID: 21924051 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]