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 *

210 related articles for article (PubMed ID: 16275254)

  • 21. Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report.
    Miano MG; Laperuta C; Chiurazzi P; D'Urso M; Ursini MV
    BMC Med Genet; 2007 Apr; 8():18. PubMed ID: 17428316
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Premature ovarian failure with FMR1 premutation, X chromosome mosaicism and blood lymphocyte microchimerism.
    Gersak K; Franic D; Veble A; Pajnic IZ; Teran N; Writzl K
    Climacteric; 2011 Apr; 14(2):289-93. PubMed ID: 20575655
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Correlation of triple repeats on the FMR1 (fragile X) gene to ovarian reserve: a new infertility test?
    Gleicher N; Weghofer A; Oktay K; Barad DH
    Acta Obstet Gynecol Scand; 2009; 88(9):1024-30. PubMed ID: 19642041
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Fragile X and reproduction.
    Martin JR; Arici A
    Curr Opin Obstet Gynecol; 2008 Jun; 20(3):216-20. PubMed ID: 18460934
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Intermediate and premutation FMR1 alleles in women with occult primary ovarian insufficiency.
    Streuli I; Fraisse T; Ibecheole V; Moix I; Morris MA; de Ziegler D
    Fertil Steril; 2009 Aug; 92(2):464-70. PubMed ID: 18973899
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [The use of DNA analysis for diagnostics of hereditary premature ovarian failure].
    Livshyts' HB; Kravchenko SA; Hryshchenko NV; Sudoma IA
    Tsitol Genet; 2005; 39(2):59-63. PubMed ID: 16161415
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry.
    Utine GE; Şimşek-Kiper PÖ; Akgün-Doğan Ö; Ürel-Demir G; Alanay Y; Aktaş D; Boduroğlu K; Tunçbilek E; Alikaşifoğlu M
    Eur J Obstet Gynecol Reprod Biol; 2018 Feb; 221():76-80. PubMed ID: 29275276
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Fragile X syndrome: premature ovarian failure. Preimplantation and preconception genetic diagnosis].
    Milà M; Mallolas J
    Rev Neurol; 2001 Oct; 33 Suppl 1():S20-3. PubMed ID: 12447814
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Abnormal function of ovaries in women carriers of premutation in the FMR1 gene].
    Lisik MZ
    Wiad Lek; 2007; 60(5-6):265-9. PubMed ID: 17966892
    [TBL] [Abstract][Full Text] [Related]  

  • 30. PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the
    Persico T; Tranquillo ML; Seracchioli R; Zuccarello D; Sorrentino U
    Genes (Basel); 2023 Dec; 15(1):. PubMed ID: 38275588
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A pilot study of premature ovarian senescence: II. Different genotype and phenotype for genetic and autoimmune etiologies.
    Gleicher N; Weghofer A; Barad DH
    Fertil Steril; 2009 May; 91(5):1707-11. PubMed ID: 18384784
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Indicators of anxiety and depression in women with the fragile X premutation: assessment of a clinical sample.
    Lachiewicz A; Dawson D; Spiridigliozzi G; Cuccaro M; Lachiewicz M; McConkie-Rosell A
    J Intellect Disabil Res; 2010 Jul; 54(7):597-610. PubMed ID: 20629912
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India.
    Guruju MR; Lavanya K; Thelma BK; Sujatha M; OmSai VR; Nagarathna V; Amarjyothi P; Jyothi A; Anandaraj MP
    J Clin Neurosci; 2009 Oct; 16(10):1305-10. PubMed ID: 19560928
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Study of FMR1 gene association with ovarian dysfunction in a sample from the Basque Country.
    Barasoain M; Barrenetxea G; Huerta I; Télez M; Carrillo A; Pérez C; Criado B; Arrieta I
    Gene; 2013 May; 521(1):145-9. PubMed ID: 23537988
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular screening of intellectually disabled patients and those with premature ovarian failure for CGG repeat expansion at FMR1 locus: Implication of combined triplet repeat primed polymerase chain reaction and methylation-specific polymerase chain reaction analysis.
    Muthuswamy S; Dean DD; Agarwal S
    Neurol India; 2016; 64(6):1175-1179. PubMed ID: 27841182
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Heterogeneity of clinical characteristics of FMR1-related disorders].
    Pereverzeva DS; Tyushkevich SA; Gorbachevskaya NL; Mamokhina UA; Danilina KK
    Zh Nevrol Psikhiatr Im S S Korsakova; 2019; 119(7):103-111. PubMed ID: 31464297
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Very early premature ovarian failure in two sisters compound heterozygous for the FMR1 premutation.
    Van Esch H; Buekenhout L; Race V; Matthijs G
    Eur J Med Genet; 2009; 52(1):37-40. PubMed ID: 19041959
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice.
    Lu C; Lin L; Tan H; Wu H; Sherman SL; Gao F; Jin P; Chen D
    Hum Mol Genet; 2012 Dec; 21(23):5039-47. PubMed ID: 22914733
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Curvilinear association of CGG repeats and age at menopause in women with FMR1 premutation expansions.
    Mailick MR; Hong J; Greenberg J; Smith L; Sherman S
    Am J Med Genet B Neuropsychiatr Genet; 2014 Dec; 165B(8):705-11. PubMed ID: 25346430
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues.
    Mandel JL; Biancalana V
    Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801
    [TBL] [Abstract][Full Text] [Related]  

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