159 related articles for article (PubMed ID: 33724218)
21. Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.
He J; Zhang QJ; Lin QF; Chen YF; Lin XZ; Lin MT; Murong SX; Wang N; Chen WJ
Gene; 2013 Apr; 518(2):325-9. PubMed ID: 23352792
[TBL] [Abstract][Full Text] [Related]
22. An Ashkenazi Jewish SMN1 haplotype specific to duplication alleles improves pan-ethnic carrier screening for spinal muscular atrophy.
Luo M; Liu L; Peter I; Zhu J; Scott SA; Zhao G; Eversley C; Kornreich R; Desnick RJ; Edelmann L
Genet Med; 2014 Feb; 16(2):149-56. PubMed ID: 23788250
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. SMN1 dosage analysis in spinal muscular atrophy from India.
Kesari A; Rennert H; Leonard DG; Mittal B
BMC Med Genet; 2005 May; 6():22. PubMed ID: 15910686
[TBL] [Abstract][Full Text] [Related]
25. Multiplex Droplet Digital PCR Method Applicable to Newborn Screening, Carrier Status, and Assessment of Spinal Muscular Atrophy.
Vidal-Folch N; Gavrilov D; Raymond K; Rinaldo P; Tortorelli S; Matern D; Oglesbee D
Clin Chem; 2018 Dec; 64(12):1753-1761. PubMed ID: 30352867
[TBL] [Abstract][Full Text] [Related]
26. Incorporating Spinal Muscular Atrophy Analysis by Next-Generation Sequencing into a Comprehensive Multigene Panel for Neuromuscular Disorders.
Tan CA; Westbrook MJ; Truty R; Kvitek DJ; Kennemer M; Winder TL; Shieh PB
Genet Test Mol Biomarkers; 2020 Oct; 24(10):616-624. PubMed ID: 32721234
[No Abstract] [Full Text] [Related]
27. [Analysis of SMN1 gene mutations in 78 patients with spinal muscular atrophy].
Li J; Zhu Y; Zhan Y; Li Y; Chen M; Wang L; He R; Zhang C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):658-661. PubMed ID: 28981927
[TBL] [Abstract][Full Text] [Related]
28. [Detection of homozygous deletions in spinal muscular atrophy with genomic DNA sequencing].
Cao YY; Qu YJ; Song F; Bai JL; Jin YW; Wang H; Li Y; Zhang WH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):410-4. PubMed ID: 23926006
[TBL] [Abstract][Full Text] [Related]
29. [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]
30. [Analysis of survival motor neuron gene conversion in patients with spinal muscular atrophy].
He SX; Ge XS; Qu YJ; Jin YW; Wang H; Bai JL; Song F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):606-11. PubMed ID: 22161088
[TBL] [Abstract][Full Text] [Related]
31. Population screening and cascade testing for carriers of SMA.
Smith M; Calabro V; Chong B; Gardiner N; Cowie S; du Sart D
Eur J Hum Genet; 2007 Jul; 15(7):759-66. PubMed ID: 17392705
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. [Genetic analysis of 90 families affected with spinal muscular atrophy].
Li T; Lyu X; Xu P; Zou J; Xiao H; Guo Q; Wang H; Liu H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Feb; 37(2):116-122. PubMed ID: 32034734
[TBL] [Abstract][Full Text] [Related]
34. Carrier frequency of spinal muscular atrophy in Thailand.
Dejsuphong D; Taweewongsounton A; Khemthong P; Chitphuk S; Stitchantrakul W; Sritara P; Tunteeratum A; Sura T
Neurol Sci; 2019 Aug; 40(8):1729-1732. PubMed ID: 31004230
[TBL] [Abstract][Full Text] [Related]
35. Diagnosis of Spinal Muscular Atrophy: A Simple Method for Quantifying the Relative Amount of Survival Motor Neuron Gene 1/2 Using Sanger DNA Sequencing.
Cao YY; Zhang WH; Qu YJ; Bai JL; Jin YW; Wang H; Song F
Chin Med J (Engl); 2018 Dec; 131(24):2921-2929. PubMed ID: 30539904
[TBL] [Abstract][Full Text] [Related]
36. [Prenatal diagnosis of spinal muscular atrophy using multiple ligation-dependent probe amplification].
Xu Y; Zhang J; Chang C; Chen S; Xu C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):214-218. PubMed ID: 33751527
[TBL] [Abstract][Full Text] [Related]
37. Molecular characterization of SMN copy number derived from carrier screening and from core families with SMA in a Chinese population.
Sheng-Yuan Z; Xiong F; Chen YJ; Yan TZ; Zeng J; Li L; Zhang YN; Chen WQ; Bao XH; Zhang C; Xu XM
Eur J Hum Genet; 2010 Sep; 18(9):978-84. PubMed ID: 20442745
[TBL] [Abstract][Full Text] [Related]
38. [Result of carrier screening for spinal muscular atrophy among 3049 reproductive-age individuals from Yunnan region].
Zhang Y; Wang L; He J; Guo J; Jin C; Tang X; Zhang J; Chen H; Zhang J; Su J; Zhu B
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):384-388. PubMed ID: 32219818
[TBL] [Abstract][Full Text] [Related]
39. Quantitative studies on SMN1 gene and carrier testing of spinal muscular atrophy.
Chen WJ; Wu ZY; Wang N; Lin MT; Mu-rong SX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):559-602. PubMed ID: 16331551
[TBL] [Abstract][Full Text] [Related]
40. [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]
[Previous] [Next] [New Search]
