187 related articles for article (PubMed ID: 34738199)
1. FMR1 allele frequencies in 51,000 newborns: a large-scale population study in China.
Zhang JY; Wu DW; Yang RL; Zhu L; Jiang MY; Wang WJ; Li XK; Jiang XL; Tong F; Shu Q
World J Pediatr; 2021 Dec; 17(6):653-658. PubMed ID: 34738199
[TBL] [Abstract][Full Text] [Related]
2. Maternal FMR1 alleles expansion in newborns during transmission: a prospective cohort study.
Shahid R; Yasin M; Rehman ZU; Jadoon H; Tahir H; Meraj N; Khan N; Zubair M; Zulfiqar I; Nowshid M; Azeem A; Jabeen M; Hameed A; Saleha S
Pediatr Res; 2023 Feb; 93(3):720-724. PubMed ID: 35681093
[TBL] [Abstract][Full Text] [Related]
3. An assessment of screening strategies for fragile X syndrome in the UK.
Pembrey ME; Barnicoat AJ; Carmichael B; Bobrow M; Turner G
Health Technol Assess; 2001; 5(7):1-95. PubMed ID: 11262423
[TBL] [Abstract][Full Text] [Related]
4. Evaluation of the human fragile X mental retardation 1 polymerase chain reaction reagents to amplify the FMR1 gene: testing in a clinical diagnostic laboratory.
Nahhas FA; Monroe TJ; Prior TW; Botma PI; Fang J; Snyder PJ; Talbott SL; Feldman GL
Genet Test Mol Biomarkers; 2012 Mar; 16(3):187-92. PubMed ID: 21992462
[TBL] [Abstract][Full Text] [Related]
5. Unstable mutations in the FMR1 gene and the phenotypes.
Loesch D; Hagerman R
Adv Exp Med Biol; 2012; 769():78-114. PubMed ID: 23560306
[TBL] [Abstract][Full Text] [Related]
6. Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: implications for fragile X syndrome carrier and newborn screening.
Hantash FM; Goos DG; Tsao D; Quan F; Buller-Burckle A; Peng M; Jarvis M; Sun W; Strom CM
Genet Med; 2010 Mar; 12(3):162-73. PubMed ID: 20168238
[TBL] [Abstract][Full Text] [Related]
7. Fragile X carrier screening and FMR1 allele distribution in the Japanese population.
Otsuka S; Sakamoto Y; Siomi H; Itakura M; Yamamoto K; Matumoto H; Sasaki T; Kato N; Nanba E
Brain Dev; 2010 Feb; 32(2):110-4. PubMed ID: 19211207
[TBL] [Abstract][Full Text] [Related]
8. Genetic cluster of fragile X syndrome in a Colombian district.
Saldarriaga W; Forero-Forero JV; González-Teshima LY; Fandiño-Losada A; Isaza C; Tovar-Cuevas JR; Silva M; Choudhary NS; Tang HT; Aguilar-Gaxiola S; Hagerman RJ; Tassone F
J Hum Genet; 2018 Apr; 63(4):509-516. PubMed ID: 29379191
[TBL] [Abstract][Full Text] [Related]
9. Maternal FMR1 premutation allele expansion and contraction in fraternal twins.
Alfaro MP; Cohen M; Vnencak-Jones CL
Am J Med Genet A; 2013 Oct; 161A(10):2620-5. PubMed ID: 23949867
[TBL] [Abstract][Full Text] [Related]
10. Diagnostic value of molecular approach in screening for fragile X premutation cases.
Refeat MM; El Saied MM; Abdel Raouf ER
Ir J Med Sci; 2023 Oct; 192(5):2265-2272. PubMed ID: 36409419
[TBL] [Abstract][Full Text] [Related]
11. Screening for
Hnoonual A; Jankittunpaiboon C; Limprasert P
Biomed Res Int; 2021; 2021():4359308. PubMed ID: 34926684
[TBL] [Abstract][Full Text] [Related]
12. FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States.
Hantash FM; Goos DM; Crossley B; Anderson B; Zhang K; Sun W; Strom CM
Genet Med; 2011 Jan; 13(1):39-45. PubMed ID: 21116185
[TBL] [Abstract][Full Text] [Related]
13. Fragile X syndrome screening in pregnant women and women planning pregnancy shows a remarkably high FMR1 premutation prevalence in the Balearic Islands.
Alfaro Arenas R; Rosell Andreo J; Heine Suñer D;
Am J Med Genet B Neuropsychiatr Genet; 2016 Dec; 171(8):1023-1031. PubMed ID: 27333191
[TBL] [Abstract][Full Text] [Related]
14. Identification of expanded alleles of the FMR1 gene among high-risk population in Indonesia by using blood spot screening.
Winarni TI; Utari A; Mundhofir FE; Tong T; Durbin-Johnson B; Faradz SM; Tassone F
Genet Test Mol Biomarkers; 2012 Mar; 16(3):162-6. PubMed ID: 21988366
[TBL] [Abstract][Full Text] [Related]
15. Polymerase chain reaction, nuclease digestion, and mass spectrometry based assay for the trinucleotide repeat status of the fragile X mental retardation 1 gene.
Dodds ED; Tassone F; Hagerman PJ; Lebrilla CB
Anal Chem; 2009 Jul; 81(13):5533-40. PubMed ID: 19514725
[TBL] [Abstract][Full Text] [Related]
16. Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.
Coffee B; Keith K; Albizua I; Malone T; Mowrey J; Sherman SL; Warren ST
Am J Hum Genet; 2009 Oct; 85(4):503-14. PubMed ID: 19804849
[TBL] [Abstract][Full Text] [Related]
17. FMR1 mRNA from full mutation alleles is associated with ABC-C
Baker EK; Arpone M; Kraan C; Bui M; Rogers C; Field M; Bretherton L; Ling L; Ure A; Cohen J; Hunter MF; Santa María L; Faundes V; Curotto B; Morales P; Trigo C; Salas I; Alliende A; Amor DJ; Godler DE
Sci Rep; 2020 Jul; 10(1):11701. PubMed ID: 32678152
[TBL] [Abstract][Full Text] [Related]
18. Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.
Tzeng CC; Tsai LP; Hwu WL; Lin SJ; Chao MC; Jong YJ; Chu SY; Chao WC; Lu CL
Am J Med Genet A; 2005 Feb; 133A(1):37-43. PubMed ID: 15637705
[TBL] [Abstract][Full Text] [Related]
19. CGG-repeat dynamics and
Zhou Y; Kumari D; Sciascia N; Usdin K
Mol Autism; 2016; 7():42. PubMed ID: 27713816
[TBL] [Abstract][Full Text] [Related]
20. Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.
Jarmolowicz AI; Baker EK; Bartlett E; Francis D; Ling L; Gamage D; Delatycki MB; Godler DE
Am J Med Genet A; 2021 May; 185(5):1498-1503. PubMed ID: 33544979
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
