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 *

59 related articles for article (PubMed ID: 7762598)

  • 21. Prenatal diagnosis of complete atrioventricular septal defect with truncus arteriosus.
    Chintala K; Gurczynski J; Aggarwal S
    Prenat Diagn; 2007 Jun; 27(6):560-2. PubMed ID: 17380467
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases.
    Weremowicz S; Sandstrom DJ; Morton CC; Niedzwiecki CA; Sandstrom MM; Bieber FR
    Prenat Diagn; 2001 Apr; 21(4):262-9. PubMed ID: 11288114
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A male case with double aneuploidy (48,XXY,+21).
    Akbas E; Soylemez F; Savasoglu K; Halliogluand O; Balci S
    Genet Couns; 2008; 19(1):59-63. PubMed ID: 18564502
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Infant with mos45,x/46,XY/47,XYY/48,XYYY: genetic and clinical findings.
    Fox JE; Blumenthal D; Brock W; Kreitzer P; Cooper R; Anderson D; Pleak R; Ehrenfreund L; Freedman S; Zaslav AL
    Am J Med Genet; 1995 Dec; 59(4):435-40. PubMed ID: 8585562
    [TBL] [Abstract][Full Text] [Related]  

  • 25. XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning.
    Fryns JP; Kleczkowska A; Kubień E; Van den Berghe H
    Genet Couns; 1995; 6(3):197-206. PubMed ID: 8588846
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis and false negative result for a case of Down syndrome with normal karyotype.
    Lizcano-Gil LA; Burgos K; Guarin DF
    Genet Couns; 2001; 12(2):167-8. PubMed ID: 11491313
    [No Abstract]   [Full Text] [Related]  

  • 27. [Prenatal diagnosis of chromosome aberrations after implementation of screening for Down's syndrome].
    Kjaergaard S; Hahnemann JM; Skibsted L; Jensen LN; Sperling L; Zingenberg H; Kristiansen A; Brøndum-Nielsen K
    Ugeskr Laeger; 2008 Mar; 170(14):1152-6. PubMed ID: 18405480
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Factors influencing parental decision making in prenatal diagnosis of sex chromosome aneuploidy.
    Mezei G; Papp C; Tóth-Pál E; Beke A; Papp Z
    Obstet Gynecol; 2004 Jul; 104(1):94-101. PubMed ID: 15229006
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Noninvasive prenatal diagnosis of aneuploidy using cell-free nucleic acids in maternal blood: promises and unanswered questions.
    Puszyk WM; Crea F; Old RW
    Prenat Diagn; 2008 Jan; 28(1):1-6. PubMed ID: 18022821
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Down syndrome in monochorionic twins.
    Sin IL; Tan TY
    Singapore Med J; 2009 Jul; 50(7):e264-7. PubMed ID: 19644615
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The XYY syndrome: a follow-up study on 38 boys.
    Geerts M; Steyaert J; Fryns JP
    Genet Couns; 2003; 14(3):267-79. PubMed ID: 14577671
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Long-term trends for socio-economic differences in prenatal diagnosis of Down syndrome: diffusion of services or persistence of disparities?
    Khoshnood B; De Vigan C; Blondel B; Vodovar V; Cadio E; Goffinet F
    BJOG; 2008 Aug; 115(9):1087-95. PubMed ID: 18518869
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Forty-two supernumerary marker chromosomes (SMCs) in 43,273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies.
    Bartsch O; Loitzsch A; Kozlowski P; Mazauric ML; Hickmann G
    Eur J Hum Genet; 2005 Nov; 13(11):1192-204. PubMed ID: 16077735
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Three cases of tetrasomy 9p.
    Dhandha S; Hogge WA; Surti U; McPherson E
    Am J Med Genet; 2002 Dec; 113(4):375-80. PubMed ID: 12457411
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings.
    Carothers AD; Boyd E; Lowther G; Ellis PM; Couzin DA; Faed MJ; Robb A
    Genet Epidemiol; 1999; 16(2):179-90. PubMed ID: 10030400
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prenatal diagnosis of 47,XXX.
    Khoury-Collado F; Wehbeh AN; Fisher AJ; Bombard AT; Weiner Z
    Am J Obstet Gynecol; 2005 May; 192(5):1469-71. PubMed ID: 15902140
    [TBL] [Abstract][Full Text] [Related]  

  • 38. At increased risk: Down syndrome relatives.
    Hecht F; Hecht BK; Wagner RC
    Ariz Med; 1983 Oct; 40(10):689-92. PubMed ID: 6228208
    [No Abstract]   [Full Text] [Related]  

  • 39. Trisomy 21 with XYY.
    Parmar RC; Muranjan MN; Swami S
    Indian J Pediatr; 2002 Nov; 69(11):979-81. PubMed ID: 12503664
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Aneuploidy and morphogenesis.
    Epstein CJ
    Prog Clin Biol Res; 1991; 373():1-18. PubMed ID: 1838180
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 3.