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Journal Abstract Search

392 related items for PubMed ID: 16970038

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  • 2. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
    Chen CP, Chern SR, Lee CC, Chang TY, Wang W, Tzen CY.
    Prenat Diagn; 2004 Jan; 24(1):38-44. PubMed ID: 14755408
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  • 3. Prenatal diagnosis of complete sole trisomy 1q.
    Pettenati MJ, Berry M, Shashi V, Hartley Bowen J, Harper M.
    Prenat Diagn; 2001 Jun; 21(6):435-40. PubMed ID: 11438944
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  • 7. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
    Machado IN, Heinrich JK, Campanhol C, Rodrigues-Peres RM, Oliveira FM, Barini R.
    Genet Mol Res; 2010 Mar 16; 9(1):441-8. PubMed ID: 20391329
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  • 11. Proximal trisomy 1q in a girl with developmental delay and minor anomalies.
    Furforo L, Rittler M, Slavutsky IR.
    Am J Med Genet; 1996 Sep 06; 64(4):551-5. PubMed ID: 8870921
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  • 12. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM.
    Am J Med Genet; 1994 Mar 01; 50(1):21-7. PubMed ID: 8160748
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  • 13. Mosaic duplication 1(q11q44) in an infant with nephroblastomatosis and mineralization of extraplacental membranes.
    Christiansen LR, Lage JM, Wolff DJ, Pai GS, Harley RA.
    Pediatr Dev Pathol; 2005 Mar 01; 8(1):115-23. PubMed ID: 15803218
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  • 14. Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?
    Reish O, Wolach B, Amiel A, Kedar I, Dolfin T, Fejgin M.
    Am J Med Genet; 1998 Apr 28; 77(1):72-5. PubMed ID: 9557898
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  • 15. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF.
    Prenat Diagn; 2005 Jun 28; 25(6):451-5. PubMed ID: 15966060
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  • 16. Constitutional partial 1q trisomy mosaicism and Wilms tumor.
    Mark HF, Wyandt H, Pan A, Milunsky JM.
    Cancer Genet Cytogenet; 2005 Oct 15; 162(2):166-71. PubMed ID: 16213366
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  • 18. Prenatal diagnosis of trisomy 1q21-qter: case report and review of literature.
    Machlitt A, Kuepferling P, Bommer C, Koerner H, Chaoui R.
    Am J Med Genet A; 2005 Apr 15; 134A(2):207-11. PubMed ID: 15704122
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  • 19. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG, Schuil J, Van Raveswaaij-Arts C, De Pater JM.
    Genet Couns; 2004 Apr 15; 15(4):405-10. PubMed ID: 15658615
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  • 20. Prenatal diagnosis of trisomy 6 mosaicism.
    Destree A, Fourneau C, Dugauquier C, Rombout S, Sartenaer D, Gillerot Y.
    Prenat Diagn; 2005 May 15; 25(5):354-7. PubMed ID: 15906424
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