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Journal Abstract Search

119 related items for PubMed ID: 14738121

  • 21. Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes.
    Chen CP, Wang PT, Lin SP, Chern SR, Chen YT, Wu PS, Kuo YL, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):120-2. PubMed ID: 24767664
    [No Abstract] [Full Text] [Related]

  • 22. Prenatal diagnosis of trisomy 6 mosaicism.
    Destree A, Fourneau C, Dugauquier C, Rombout S, Sartenaer D, Gillerot Y.
    Prenat Diagn; 2005 May; 25(5):354-7. PubMed ID: 15906424
    [Abstract] [Full Text] [Related]

  • 23. Significance of mosaic isochromosome 20q on amniocentesis.
    Donnenfeld AE, Kershner MA.
    Am J Med Genet; 1993 Dec 01; 47(8):1196-7. PubMed ID: 8291555
    [Abstract] [Full Text] [Related]

  • 24. Discrepancy between the fetus and extra-embryonic tissues in prenatally detected mosaic distal 5p deletion.
    Chen CP, Lee CC, Town DD, Lee MS, Wang W.
    Genet Couns; 2004 Dec 01; 15(4):473-6. PubMed ID: 15658625
    [Abstract] [Full Text] [Related]

  • 25. Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy.
    Chen CP, Lee CC, Chen WL, Wang W, Tzen CY.
    Prenat Diagn; 2004 Jan 01; 24(1):19-25. PubMed ID: 14755404
    [Abstract] [Full Text] [Related]

  • 26. Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism.
    Kosaki R, Hanai S, Kakishima H, Okada MA, Hayashi S, Ito Y, Takahashi T, Kosaki K, Okuyama T.
    Congenit Anom (Kyoto); 2006 Jun 01; 46(2):115-7. PubMed ID: 16732770
    [Abstract] [Full Text] [Related]

  • 27. Accuracy of perinatal diagnosis of 45,X/46,XY mosaicism and electronic consultation of affected parents.
    Kibar Y, Frimberger D, Kropp BP, Reiner W.
    J Pediatr Urol; 2009 Aug 01; 5(4):274-8. PubMed ID: 19329364
    [Abstract] [Full Text] [Related]

  • 28. Prenatal identification of a marker chromosome 16 by chromosome microdissection and reverse FISH.
    de Pater J, Van der Sijs-Bos C, Prins M, Derks J, Albrechts J, Engelen J.
    Eur J Med Genet; 2006 Aug 01; 49(4):306-12. PubMed ID: 16461028
    [Abstract] [Full Text] [Related]

  • 29. Dandy-Walker malformation in a male fetus with mosaic 45,X/46,X,del(Y)(q11).
    Witters I, Vandecruys H, Devlieger R, Fryns JP.
    Genet Couns; 2008 Aug 01; 19(4):439-41. PubMed ID: 19239090
    [No Abstract] [Full Text] [Related]

  • 30. Prenatal diagnosis of a mosaic supernumerary marker iso (8p) (tetrasomy 8p): discordance between chorionic villi culture and amniotic fluid karyotypes.
    Nucaro AL, Rossino R, Pruna D, Rassu S, Cianchetti C, Cao A, Moi P.
    Prenat Diagn; 2006 May 01; 26(5):418-9. PubMed ID: 16532523
    [Abstract] [Full Text] [Related]

  • 31. Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis.
    Chen CP, Chang TY, Chern SR, Lee CC, Town DD, Lee MS, Wang W.
    Prenat Diagn; 2007 Apr 01; 27(4):383-5. PubMed ID: 17393556
    [No Abstract] [Full Text] [Related]

  • 32. Mosaic trisomy 20: considerations for genetic counseling.
    Bianca S, Boemi G, Barrano B, Cataliotti A, Ingegnosi C, Indaco L, Ettore G.
    Am J Med Genet A; 2008 Jul 15; 146A(14):1897-8. PubMed ID: 18553567
    [No Abstract] [Full Text] [Related]

  • 33. Structural chromosomal mosaicism and prenatal diagnosis.
    Pipiras E, Dupont C, Chantot-Bastaraud S, Siffroi JP, Bucourt M, Batallan A, Largillière C, Uzan M, Wolf JP, Benzacken B.
    Prenat Diagn; 2004 Feb 15; 24(2):101-3. PubMed ID: 14974115
    [Abstract] [Full Text] [Related]

  • 34. Second-trimester genetic amniocentesis: 5-year experience.
    Turhan NO, Eren U, Seçkin NC.
    Arch Gynecol Obstet; 2005 Jan 15; 271(1):19-21. PubMed ID: 15290165
    [Abstract] [Full Text] [Related]

  • 35. Maternal uniparental disomy 16 and genetic counseling: new case and survey of published cases.
    Eggermann T, Curtis M, Zerres K, Hughes HE.
    Genet Couns; 2004 Jan 15; 15(2):183-90. PubMed ID: 15287418
    [Abstract] [Full Text] [Related]

  • 36. Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis.
    Chen CP, Chern SR, Chen LF, Chen WL, Wang W.
    Prenat Diagn; 2005 Nov 15; 25(11):1067-9. PubMed ID: 16302164
    [No Abstract] [Full Text] [Related]

  • 37. Prenatal diagnosis of the distal 11q deletion and review of the literature.
    Chen CP, Chern SR, Chang TY, Tzen CY, Lee CC, Chen WL, Chen LF, Wang W.
    Prenat Diagn; 2004 Feb 15; 24(2):130-6. PubMed ID: 14974122
    [Abstract] [Full Text] [Related]

  • 38. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A, Kitsiou S, Fryssira H, Sofocleous C, Kouvidi E, Tsangaris GT, Salavoura K, Mavrou A.
    In Vivo; 2006 Feb 15; 20(4):473-8. PubMed ID: 16900777
    [Abstract] [Full Text] [Related]

  • 39. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
    Hartmann A, Hofmann UB, Hoehn H, Broecker EB, Hamm H.
    Pediatr Dermatol; 2004 Feb 15; 21(6):636-41. PubMed ID: 15575846
    [Abstract] [Full Text] [Related]

  • 40. Prenatally detected trisomy 20 mosaicism.
    Robinson WP, McGillivray B, Lewis ME, Arbour L, Barrett I, Kalousek DK.
    Prenat Diagn; 2005 Mar 15; 25(3):239-44. PubMed ID: 15791659
    [Abstract] [Full Text] [Related]

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