70 related articles for article (PubMed ID: 15608400)
1. Quantitative analysis of SMN1 gene and estimation of SMN1 deletion carrier frequency in Korean population based on real-time PCR.
Lee TM; Kim SW; Lee KS; Jin HS; Koo SK; Jo I; Kang S; Jung SC
J Korean Med Sci; 2004 Dec; 19(6):870-3. PubMed ID: 15608400
[TBL] [Abstract][Full Text] [Related]
2. Assessment of Spinal Muscular Atrophy Carrier Status by Determining
Wijaya YOS; Purevsuren J; Harahap NIF; Niba ETE; Bouike Y; Nurputra DK; Rochmah MA; Thursina C; Hapsara S; Yamaguchi S; Nishio H; Shinohara M
Int J Neonatal Screen; 2020 Jun; 6(2):43. PubMed ID: 33073034
[TBL] [Abstract][Full Text] [Related]
3. Carrier screening for spinal muscular atrophy in 22913 Chinese reproductive age women.
Zhang L; Mo J; Zhou L; Xu X; Xu Z; Zhang L; Wu W
Mol Genet Genomic Med; 2024 Jan; 12(1):e2359. PubMed ID: 38284446
[TBL] [Abstract][Full Text] [Related]
4. A multi-source approach to determine SMA incidence and research ready population.
Verhaart IEC; Robertson A; Leary R; McMacken G; König K; Kirschner J; Jones CC; Cook SF; Lochmüller H
J Neurol; 2017 Jul; 264(7):1465-1473. PubMed ID: 28634652
[TBL] [Abstract][Full Text] [Related]
5. Analysis of spinal muscular atrophy carrier screening results in 32,416 pregnant women and 7,231 prepregnant women.
Zhou BB; Chen X; Zhang C; Wang YP; Ma PP; Hao SJ; Hui L; Bai YF
Front Neurol; 2024; 15():1357476. PubMed ID: 38654739
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Comprehensive Analysis of Spinal Muscular Atrophy: SMN1 Copy Number, Intragenic Mutation, and 2 + 0 Carrier Analysis by Third-Generation Sequencing.
Li S; Han X; Xu Y; Chang C; Gao L; Li J; Lu Y; Mao A; Wang Y
J Mol Diagn; 2022 Sep; 24(9):1009-1020. PubMed ID: 35659528
[TBL] [Abstract][Full Text] [Related]
9. Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy.
Mendell JR; Al-Zaidy S; Shell R; Arnold WD; Rodino-Klapac LR; Prior TW; Lowes L; Alfano L; Berry K; Church K; Kissel JT; Nagendran S; L'Italien J; Sproule DM; Wells C; Cardenas JA; Heitzer MD; Kaspar A; Corcoran S; Braun L; Likhite S; Miranda C; Meyer K; Foust KD; Burghes AHM; Kaspar BK
N Engl J Med; 2017 Nov; 377(18):1713-1722. PubMed ID: 29091557
[TBL] [Abstract][Full Text] [Related]
10. Carrier screening for spinal muscular atrophy.
Prior TW;
Genet Med; 2008 Nov; 10(11):840-2. PubMed ID: 18941424
[No Abstract] [Full Text] [Related]
11. NAIP Gene Deletion and SMN2 Copy Number as Molecular Tools in Predicting the Severity of Spinal Muscular Atrophy.
Abd El Mutaleb ANH; Ibrahim FAR; Megahed FAK; Atta A; Ali BA; Omar TEI; Rashad MM
Biochem Genet; 2024 Feb; ():. PubMed ID: 38388850
[TBL] [Abstract][Full Text] [Related]
12. Carrier frequency of Spino-muscular atrophy in individuals of a reproductive age group from North India.
Kaur A; Kumari A; Kaur A; Sharma R; Srivastava P; Suthar R
J Family Med Prim Care; 2022 Dec; 11(12):7870-7874. PubMed ID: 36994015
[TBL] [Abstract][Full Text] [Related]
13. New-Born Screening for Spinal Muscular Atrophy: Results of a Latvian Pilot Study.
Gailite L; Sterna O; Konika M; Isakovs A; Isakova J; Micule I; Setlere S; Diriks M; Auzenbaha M
Int J Neonatal Screen; 2022 Feb; 8(1):. PubMed ID: 35225937
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Carrier Frequency of Spinal Muscular Atrophy in a Large-scale Korean Population.
Park JE; Yun SA; Roh EY; Yoon JH; Shin S; Ki CS
Ann Lab Med; 2020 Jul; 40(4):326-330. PubMed ID: 32067433
[TBL] [Abstract][Full Text] [Related]
16. Prevalence, incidence and carrier frequency of 5q-linked spinal muscular atrophy - a literature review.
Verhaart IEC; Robertson A; Wilson IJ; Aartsma-Rus A; Cameron S; Jones CC; Cook SF; Lochmüller H
Orphanet J Rare Dis; 2017 Jul; 12(1):124. PubMed ID: 28676062
[TBL] [Abstract][Full Text] [Related]
17. Assessment of DPY19L2 Deletion in Familial and Non-Familial Individuals with Globozoospermia and DPY19L2 Genotyping.
Modarres P; Tanhaei S; Tavalaee M; Ghaedi K; Deemeh MR; Nasr-Esfahani MH
Int J Fertil Steril; 2016; 10(2):196-207. PubMed ID: 27441053
[TBL] [Abstract][Full Text] [Related]
18. Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa.
Sangaré M; Hendrickson B; Sango HA; Chen K; Nofziger J; Amara A; Dutra A; Schindler AB; Guindo A; Traoré M; Harmison G; Pak E; Yaro FN; Bricceno K; Grunseich C; Chen G; Boehm M; Zukosky K; Bocoum N; Meilleur KG; Daou F; Bagayogo K; Coulibaly YI; Diakité M; Fay MP; Lee HS; Saad A; Gribaa M; Singleton AB; Maiga Y; Auh S; Landouré G; Fairhurst RM; Burnett BG; Scholl T; Fischbeck KH
Ann Neurol; 2014 Apr; 75(4):525-32. PubMed ID: 24515897
[TBL] [Abstract][Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
