BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

353 related articles for article (PubMed ID: 28253484)

  • 21. Molecular Characterization of FMR1 Gene by TP-PCR in Women of Reproductive Age and Women with Premature Ovarian Insufficiency.
    Dean DD; Agarwal S; Kapoor D; Singh K; Vati C
    Mol Diagn Ther; 2018 Feb; 22(1):91-100. PubMed ID: 29188551
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Mosaicism for FMR1 gene full mutation and intermediate allele in a female foetus: a postzygotic retraction event.
    Ferreira SI; Pires LM; Ferrão J; Sá J; Serra A; Carreira IM
    Gene; 2013 Sep; 527(1):421-5. PubMed ID: 23792063
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers.
    Nolin SL; Glicksman A; Ersalesi N; Dobkin C; Brown WT; Cao R; Blatt E; Sah S; Latham GJ; Hadd AG
    Genet Med; 2015 May; 17(5):358-64. PubMed ID: 25210937
    [TBL] [Abstract][Full Text] [Related]  

  • 25. FMR1 CGG repeat lengths mediate different regulation of reporter gene expression in comparative transient and locus specific integration assays.
    Sølvsten C; Nielsen AL
    Gene; 2011 Oct; 486(1-2):15-22. PubMed ID: 21767618
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.
    Tassone F; Pan R; Amiri K; Taylor AK; Hagerman PJ
    J Mol Diagn; 2008 Jan; 10(1):43-9. PubMed ID: 18165273
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile.
    Santa María L; Aliaga S; Faundes V; Morales P; Pugin Á; Curotto B; Soto P; Peña MI; Salas I; Alliende MA
    Genet Res (Camb); 2016 Jun; 98():e11. PubMed ID: 27350105
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population.
    Sharma D; Gupta M; Thelma BK
    Genet Epidemiol; 2001 Jan; 20(1):129-144. PubMed ID: 11119302
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Triplet expansion cytosine-guanine-guanine: Three cases of OMIM syndrome in the same family].
    González-Pérez J; Izquierdo-Álvarez S; Fuertes-Rodrigo C; Monge-Galindo L; Peña-Segura JL; López-Pisón FJ
    Med Clin (Barc); 2016 Apr; 146(7):311-5. PubMed ID: 26776484
    [TBL] [Abstract][Full Text] [Related]  

  • 31. FMR1 gene mutation screening by TP-PCR in patients with premature ovarian failure and fragile-X.
    Tural S; Tekcan A; Kara N; Elbistan M; Güven D; Ali Tasdemir H
    Gynecol Endocrinol; 2015 Mar; 31(3):191-5. PubMed ID: 25366135
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. Newborn, carrier, and early childhood screening recommendations for fragile X.
    Abrams L; Cronister A; Brown WT; Tassone F; Sherman SL; Finucane B; McConkie-Rosell A; Hagerman R; Kaufmann WE; Picker J; Coffey S; Skinner D; Johnson V; Miller R; Berry-Kravis E
    Pediatrics; 2012 Dec; 130(6):1126-35. PubMed ID: 23129072
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Diminished ovarian reserve is not observed in infertility patients with high normal CGG repeats on the fragile X mental retardation 1 (FMR1) gene.
    Schufreider A; McQueen DB; Lee SM; Allon R; Uhler ML; Davie J; Feinberg EC
    Hum Reprod; 2015 Nov; 30(11):2686-92. PubMed ID: 26345686
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Population-based carrier screening and prenatal diagnosis of fragile X syndrome in East Asian populations.
    Guo Q; Chang YY; Huang CH; Hsiao YS; Hsiao YC; Chiu IF; Zhou Y; Zhang H; Ko TM
    J Genet Genomics; 2021 Dec; 48(12):1104-1110. PubMed ID: 34412977
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation.
    Kallinen J; Heinonen S; Mannermaa A; Ryynänen M
    Clin Genet; 2000 Aug; 58(2):111-5. PubMed ID: 11005143
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Prenatal diagnosis for 30 women carrying a FMR1 mutation].
    Huang W; Xue J; Kang H; Guan X; Teng Y; Wu L; Duan R
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Sep; 36(9):866-869. PubMed ID: 31515777
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Analysis and prenatal diagnosis of FMR1 gene mutations among patients with unexplained mental retardation].
    Luo S; He W; Liao Y; Tang W; Li X; Hu L; Du J; Zhang Q; Tan Y; Lin G; Li W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 May; 38(5):439-445. PubMed ID: 33974251
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The prevalence of CGG repeat expansion mutation in FMR1 gene in the northern Chinese women of reproductive age.
    Ma Y; Wei X; Pan H; Wang S; Wang X; Liu X; Zou L; Wang X; Wang X; Yang H; Wang F; Wang K; Sun L; Qiao X; Yang Y; Ma X; Liu D; Ding G; Ma J; Yang X; Zhu S; Qi Y; Yin C
    BMC Med Genet; 2019 May; 20(1):81. PubMed ID: 31096929
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.