BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 20398889)

  • 1. Premature ovarian failure and FMR1 gene mutations: an update.
    Conway GS
    Ann Endocrinol (Paris); 2010 May; 71(3):215-7. PubMed ID: 20398889
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The FMR1 premutation and reproduction.
    Wittenberger MD; Hagerman RJ; Sherman SL; McConkie-Rosell A; Welt CK; Rebar RW; Corrigan EC; Simpson JL; Nelson LM
    Fertil Steril; 2007 Mar; 87(3):456-65. PubMed ID: 17074338
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fragile X premutation screening in women with premature ovarian failure.
    Conway GS; Payne NN; Webb J; Murray A; Jacobs PA
    Hum Reprod; 1998 May; 13(5):1184-7. PubMed ID: 9647544
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations.
    Beke A; Piko H; Haltrich I; Karcagi V; Rigo J; Molnar MJ; Fekete G
    BMC Med Genet; 2018 Jul; 19(1):113. PubMed ID: 29986653
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Analysis of FMR1 gene premutation and X chromosome cytogenetic abnormalities in 100 Tunisian patients presenting premature ovarian failure.
    Bouali N; Hmida D; Mougou S; Bouligand J; Lakhal B; Dimessi S; Francou B; Saad G; Trabelsi S; Zaouali M; Gribaa M; Chaieb M; Bibi M; Guiochon-Mantel A; Saad A
    Ann Endocrinol (Paris); 2015 Dec; 76(6):671-8. PubMed ID: 26593861
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A woman with spontaneous premature ovarian failure gives birth to a child with fragile X syndrome.
    Corrigan EC; Raygada MJ; Vanderhoof VH; Nelson LM
    Fertil Steril; 2005 Nov; 84(5):1508. PubMed ID: 16275254
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers.
    Ennis S; Ward D; Murray A
    Eur J Hum Genet; 2006 Feb; 14(2):253-5. PubMed ID: 16251893
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Premature ovarian failure and FRAXA premutation: Positive correlation in a Brazilian survey.
    Machado-Ferreira Mdo C; Costa-Lima MA; Boy RT; Esteves GS; Pimentel MM
    Am J Med Genet A; 2004 Apr; 126A(3):237-40. PubMed ID: 15054835
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X chromosome inactivation does not define the development of premature ovarian failure in fragile X premutation carriers.
    Spath MA; Nillesen WN; Smits AP; Feuth TB; Braat DD; van Kessel AG; Yntema HG
    Am J Med Genet A; 2010 Feb; 152A(2):387-93. PubMed ID: 20101683
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Association between idiopathic premature ovarian failure and fragile X premutation.
    Marozzi A; Vegetti W; Manfredini E; Tibiletti MG; Testa G; Crosignani PG; Ginelli E; Meneveri R; Dalprà L
    Hum Reprod; 2000 Jan; 15(1):197-202. PubMed ID: 10611212
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Studies of FRAXA and FRAXE in women with premature ovarian failure.
    Murray A; Webb J; Grimley S; Conway G; Jacobs P
    J Med Genet; 1998 Aug; 35(8):637-40. PubMed ID: 9719368
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [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]  

  • 19. The significance of fragile X mental retardation gene 1 CGG repeat sizes in the normal and intermediate range in women with primary ovarian insufficiency.
    Voorhuis M; Onland-Moret NC; Janse F; Ploos van Amstel HK; Goverde AJ; Lambalk CB; Laven JS; van der Schouw YT; Broekmans FJ; Fauser BC;
    Hum Reprod; 2014 Jul; 29(7):1585-93. PubMed ID: 24812319
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Premutations of FMR1 CGG repeats are not related to idiopathic premature ovarian failure in Iranian patients: A case control study.
    Asadi R; Omrani MD; Ghaedi H; Mirfakhraie R; Azargashb E; Habibi M; Pouresmaeili F
    Gene; 2018 Nov; 676():189-194. PubMed ID: 30030199
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.