BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 22095609)

  • 21. Preimplantation genetic diagnosis of Morquio disease.
    Qubbaj W; Al-Aqeel AI; Al-Hassnan Z; Al-Duraihim A; Awartani K; Al-Rejjal R; Coskun S
    Prenat Diagn; 2008 Oct; 28(10):900-3. PubMed ID: 18792995
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
    Cronister A; Teicher J; Rohlfs EM; Donnenfeld A; Hallam S
    Obstet Gynecol; 2008 Mar; 111(3):596-601. PubMed ID: 18310361
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease.
    Handyside AH; Robinson MD; Simpson RJ; Omar MB; Shaw MA; Grudzinskas JG; Rutherford A
    Mol Hum Reprod; 2004 Oct; 10(10):767-72. PubMed ID: 15322224
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutation and haplotype analysis for Duchenne muscular dystrophy by single cell multiple displacement amplification.
    Ren Z; Zhou C; Xu Y; Deng J; Zeng H; Zeng Y
    Mol Hum Reprod; 2007 Jun; 13(6):431-6. PubMed ID: 17439955
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The effect of CGG repeat number on ovarian response among fragile X premutation carriers undergoing preimplantation genetic diagnosis.
    Bibi G; Malcov M; Yuval Y; Reches A; Ben-Yosef D; Almog B; Amit A; Azem F
    Fertil Steril; 2010 Aug; 94(3):869-74. PubMed ID: 19481741
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Multiplex methylation specific PCR analysis of fragile X syndrome: experience in Songklanagarind Hospital.
    Charalsawadi C; Sripo T; Limprasert P
    J Med Assoc Thai; 2005 Aug; 88(8):1057-61. PubMed ID: 16404832
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Chromosome fragility at FRAXA in human cleavage stage embryos at risk for fragile X syndrome.
    Verdyck P; Berckmoes V; De Vos A; Verpoest W; Liebaers I; Bonduelle M; De Rycke M
    Am J Med Genet A; 2015 Oct; 167A(10):2306-13. PubMed ID: 25953684
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fragile X founder effects and new mutations in Finland.
    Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; Wang D; Ju W; Nolin S; Dobkin C; Ryynänen M; Brown WT
    Am J Med Genet; 1996 Jul; 64(1):226-33. PubMed ID: 8826481
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fragile X-associated tremor/ataxia syndrome: intrafamilial variability and the size of the FMR1 premutation CGG repeat.
    Capelli LP; Gonçalves MR; Kok F; Leite CC; Nitrini R; Barbosa ER; Vianna-Morgante AM
    Mov Disord; 2007 Apr; 22(6):866-70. PubMed ID: 17290448
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Diagnostic testing in fragile X syndrome].
    Sireteanu A; Rusu C
    Rev Med Chir Soc Med Nat Iasi; 2006; 110(4):968-71. PubMed ID: 17438909
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular diagnosis of Fragile X syndrome.
    Sofocleous C; Kolialexi A; Mavrou A
    Expert Rev Mol Diagn; 2009 Jan; 9(1):23-30. PubMed ID: 19099346
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Successful preimplantation genetic diagnosis for beta-thalassemia using multiplex nested polymerase chain reaction].
    Deng J; Zhuang GL; Peng WL; Zhou CQ; Li J; Liang XY; Deng MF; Zeng YH; Sun HY
    Zhonghua Yi Xue Za Zhi; 2005 Mar; 85(12):811-5. PubMed ID: 15949396
    [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. Clinical application of multiple displacement amplification in preimplantation genetic diagnosis.
    Hellani A; Coskun S; Tbakhi A; Al-Hassan S
    Reprod Biomed Online; 2005 Mar; 10(3):376-80. PubMed ID: 15820046
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Closely linked polymorphic marker: successful application in preimplantation genetic diagnosis for beta-thalassemia.
    Deng J; Zhuang GL; Peng WL; Zhou CQ; Li J; Fang C; Li SP; Chen Y; Tong DY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):391-5. PubMed ID: 16086275
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population.
    Jara L; Aspillaga M; Avendaño I; Obreque V; Blanco R; Valenzuela CY
    Am J Med Genet; 1998 Jan; 75(3):277-82. PubMed ID: 9475597
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Results from 10 years of preimplantation-genetic diagnostics in The Netherlands].
    de Die-Smulders CE; Land JA; Dreesen JC; Coonen E; Evers JL; Geraedts JP
    Ned Tijdschr Geneeskd; 2004 Dec; 148(50):2491-6. PubMed ID: 15638197
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel duplication in the FMR1 gene: implications for molecular analysis in fragile X syndrome and repeat instability.
    Mononen T; von Koskull H; Airaksinen RL; Juvonen V
    Clin Genet; 2007 Dec; 72(6):528-31. PubMed ID: 17922850
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia.
    Larsen LA; Vuust J; Nystad M; Evseeva I; Van Ghelue M; Tranebjaerg L
    Eur J Hum Genet; 2001 Sep; 9(9):724-7. PubMed ID: 11571563
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.