These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

204 related articles for article (PubMed ID: 24395328)

  • 21. Newborn screening for fragile X syndrome.
    Bailey DB
    Ment Retard Dev Disabil Res Rev; 2004; 10(1):3-10. PubMed ID: 14994282
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. Screening for Fragile X Syndrome Among Filipino Children with Autism Spectrum Disorder.
    Dy ABC; Tanchanco LBS; Sy JCY; Levantino MD; Hagerman RJ
    J Autism Dev Disord; 2023 Nov; 53(11):4465-4473. PubMed ID: 35972625
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Incidence of fragile X in 5,000 consecutive newborn males.
    Rifé M; Badenas C; Mallolas J; Jiménez L; Cervera R; Maya A; Glover G; Rivera F; Milà M
    Genet Test; 2003; 7(4):339-43. PubMed ID: 15000813
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Pilot fragile X screening in normal population of Taiwan.
    Tzeng CC; Cho WC; Kuo PL; Chen RM
    Diagn Mol Pathol; 1999 Sep; 8(3):152-6. PubMed ID: 10565687
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [FMR1 PREMUTATION CARRIERS - ARE THEY REALLY ASYMPTOMATIC?].
    Elizur S; Berkenstadt M; Ries-Levavi L; Gruber N; Pinhas-Hamiel O; Hassin-Baer S; Raas-Rothschild A; Raanani H; Cukierman-Yaffe T; Orvieto R; Cohen Y; Gabis L
    Harefuah; 2018 Apr; 157(4):241-244. PubMed ID: 29688643
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fragile X syndrome prenatal diagnosis: parental attitudes and reproductive responses.
    Xunclà M; Badenas C; Domínguez M; Rodríguez-Revenga L; Madrigal I; Jiménez L; Soler A; Borrell A; Sánchez A; Milà M
    Reprod Biomed Online; 2010 Oct; 21(4):560-5. PubMed ID: 20801083
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy.
    Gao F; Huang W; You Y; Huang J; Zhao J; Xue J; Kang H; Zhu Y; Hu Z; Allen EG; Jin P; Xia K; Duan R
    Mol Genet Genomic Med; 2020 Jun; 8(6):e1236. PubMed ID: 32281281
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Climbing the branches of a family tree: diagnosis of fragile X syndrome.
    Visootsak J; Hipp H; Clark H; Berry-Kravis E; Anderson T; Laney D
    J Pediatr; 2014 Jun; 164(6):1292-5. PubMed ID: 24612903
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Coexistence of Fragile-X Syndrome, 8p23.1 Deletion, and Balanced Translocation t(7;10)(p10;q24) in a Single Family.
    Cortés H; Reyes-Rosales M; Rojas-Velasco AJ; García-Juárez B; Tapia-Guerrero YS; Arenas-Diaz S; Leyva-García N; Macías-Gallardo JJ; Carrillo-Mora P; Magaña JJ
    Genet Test Mol Biomarkers; 2020 Aug; 24(8):527-531. PubMed ID: 32716213
    [No Abstract]   [Full Text] [Related]  

  • 34. 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]  

  • 35. 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]  

  • 36. 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]  

  • 37. Fragile X premutation and associated health conditions: A review.
    Tassanakijpanich N; Hagerman RJ; Worachotekamjorn J
    Clin Genet; 2021 Jun; 99(6):751-760. PubMed ID: 33443313
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cascade Screening for Fragile X Syndrome/CGG Repeat Expansions in Children Attending Special Education in Sri Lanka.
    Chandrasekara CH; Wijesundera WS; Perera HN; Chong SS; Rajan-Babu IS
    PLoS One; 2015; 10(12):e0145537. PubMed ID: 26694146
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation.
    Farzin F; Perry H; Hessl D; Loesch D; Cohen J; Bacalman S; Gane L; Tassone F; Hagerman P; Hagerman R
    J Dev Behav Pediatr; 2006 Apr; 27(2 Suppl):S137-44. PubMed ID: 16685180
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.