407 related articles for article (PubMed ID: 21364876)
1. Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study.
Su YN; Hung CC; Lin SY; Chen FY; Chern JP; Tsai C; Chang TS; Yang CC; Li H; Ho HN; Lee CN
PLoS One; 2011 Feb; 6(2):e17067. PubMed ID: 21364876
[TBL] [Abstract][Full Text] [Related]
2. [Carrier screening for spinal muscular atrophy in 4719 pregnant women in Shanghai region].
Gong B; Zhang L; Hou YP; Hu HY; Li HC; Tan MY; Chen J; Yu J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):670-2. PubMed ID: 24327144
[TBL] [Abstract][Full Text] [Related]
3. Carrier Screening and Prenatal Diagnosis for Spinal Muscular Atrophy in 13,069 Chinese Pregnant Women.
Zhang J; Wang Y; Ma D; Sun Y; Li Y; Yang P; Luo C; Jiang T; Hu P; Xu Z
J Mol Diagn; 2020 Jun; 22(6):817-822. PubMed ID: 32205292
[TBL] [Abstract][Full Text] [Related]
4. [Screening for spinal muscular atrophy mutation carriers among 4931 pregnant women from Liuzhou region of Guangxi].
Tan J; Zhang X; Wang Y; Luo S; Yang F; Liu B; Cai R
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):467-470. PubMed ID: 30098235
[TBL] [Abstract][Full Text] [Related]
5. Preconception or prenatal acceptance of SMN1 gene carrier screening and carrier rate of spinal muscular atrophy: a retrospective study in 18,818 reproductive age women in Wuhan area of China.
Sun Y; Ma S; Xiao J; Wu J; Wu Y; Shi X; Li S; Feng L; Chen S
J Assist Reprod Genet; 2024 Jan; 41(1):127-133. PubMed ID: 37991656
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene.
Alías L; Barceló MJ; Bernal S; Martínez-Hernández R; Also-Rallo E; Vázquez C; Santana A; Millán JM; Baiget M; Tizzano EF
Clin Genet; 2014 May; 85(5):470-5. PubMed ID: 23799925
[TBL] [Abstract][Full Text] [Related]
8. Spinal muscular atrophy carriers with two SMN1 copies.
Ar Rochmah M; Awano H; Awaya T; Harahap NIF; Morisada N; Bouike Y; Saito T; Kubo Y; Saito K; Lai PS; Morioka I; Iijima K; Nishio H; Shinohara M
Brain Dev; 2017 Nov; 39(10):851-860. PubMed ID: 28676237
[TBL] [Abstract][Full Text] [Related]
9. Genetic carrier screening for spinal muscular atrophy and spinal muscular atrophy with respiratory distress 1 in an isolated population in Israel.
Basel-Vanagaite L; Taub E; Drasinover V; Magal N; Brudner A; Zlotogora J; Shohat M
Genet Test; 2008 Mar; 12(1):53-6. PubMed ID: 18298318
[TBL] [Abstract][Full Text] [Related]
10. Carrier frequency of SMN1-related spinal muscular atrophy in north Indian population: The need for population based screening program.
Nilay M; Moirangthem A; Saxena D; Mandal K; Phadke SR
Am J Med Genet A; 2021 Jan; 185(1):274-277. PubMed ID: 33051992
[TBL] [Abstract][Full Text] [Related]
11. Carrier Screening and Diagnosis for Spinal Muscular Atrophy Using Droplet Digital PCR Versus MLPA: Analytical Validation and Early Test Outcome.
Shekhawat DS; Didel S; Dixit SG; Singh P; Singh K
Genet Test Mol Biomarkers; 2024 May; 28(5):207-212. PubMed ID: 38533877
[No Abstract] [Full Text] [Related]
12. Screening and prenatal diagnosis of survival motor neuron gene deletion in pregnant women in Zhaoqing city, Guangdong Province.
Huang Z; Yang Q; Ye J; Huang J; Lin J; Chen J; Liang Z; Cao Z
BMC Med Genomics; 2023 Mar; 16(1):39. PubMed ID: 36859245
[TBL] [Abstract][Full Text] [Related]
13. [Results of carrier screening for Spinal muscular atrophy among 35 145 reproductive-aged individuals from Dongguan region].
Zhao Y; Lou J; Fu Y; Dai Y; Liang Q; Sun M; Tan J; Liu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jun; 40(6):655-660. PubMed ID: 37211998
[TBL] [Abstract][Full Text] [Related]
14. Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72,400 specimens.
Sugarman EA; Nagan N; Zhu H; Akmaev VR; Zhou Z; Rohlfs EM; Flynn K; Hendrickson BC; Scholl T; Sirko-Osadsa DA; Allitto BA
Eur J Hum Genet; 2012 Jan; 20(1):27-32. PubMed ID: 21811307
[TBL] [Abstract][Full Text] [Related]
15. The clinical utility of a risk-modifying SNP to detect carriers for spinal muscular atrophy with increased sensitivity.
Ware G; Miller C; Jones D; Avenarius M
Mol Genet Genomic Med; 2022 Apr; 10(4):e1897. PubMed ID: 35289093
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. SMN1 gene copy number analysis for spinal muscular atrophy (SMA) in a Turkish cohort by CODE-SEQ technology, an integrated solution for detection of SMN1 and SMN2 copy numbers and the "2+0" genotype.
Ceylan AC; Erdem HB; Şahin İ; Agarwal M
Neurol Sci; 2020 Sep; 41(9):2575-2584. PubMed ID: 32249332
[TBL] [Abstract][Full Text] [Related]
20. Carrier frequency of SMA by quantitative analysis of the SMN1 deletion in the Iranian population.
Hasanzad M; Azad M; Kahrizi K; Saffar BS; Nafisi S; Keyhanidoust Z; Azimian M; Refah AA; Also E; Urtizberea JA; Tizzano EF; Najmabadi H
Eur J Neurol; 2010 Jan; 17(1):160-2. PubMed ID: 19538222
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
