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Journal Abstract Search

120 related items for PubMed ID: 3812567

  • 1. Prenatal diagnosis of a dup(3p) with holoprosencephaly.
    Gillerot Y, Hustin J, Koulischer L, Viteux V.
    Am J Med Genet; 1987 Jan; 26(1):225-7. PubMed ID: 3812567
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  • 4. Dup(3)(p2----pter) in two families, including one infant with cyclopia.
    Gimelli G, Cuoco C, Lituania M, Cordone M, Aricò M, Bianchi E, Maraschio P, Zuffardi O.
    Am J Med Genet; 1985 Feb; 20(2):341-8. PubMed ID: 3919583
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  • 5. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
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  • 6. Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.
    Chen CP, Liu FF, Jan SW, Lin SP, Lan CC.
    Prenat Diagn; 1996 Mar; 16(3):270-5. PubMed ID: 8710784
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  • 11. Duplication 3p21----3pter and cyclopia.
    Kurtzman DN, Van Dyke DL, Rich CA, Weiss L.
    Am J Med Genet; 1987 May; 27(1):33-7. PubMed ID: 3605204
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  • 15. [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ].
    Balícek P, Jüttnerová V, Jarosová M, Fialová J, Fiedler Z, Kolmanová J.
    Cas Lek Cesk; 2001 Mar 01; 140(4):122-4. PubMed ID: 11284430
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  • 16. Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p.
    Le Caignec C, Winer N, Boceno M, Delnatte C, Podevin G, Liet JM, Quere MP, Joubert M, Rival JM.
    Prenat Diagn; 2003 Dec 15; 23(12):981-4. PubMed ID: 14663834
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  • 17. Holoprosencephaly: examples of clinical variability and etiologic heterogeneity.
    Corsello G, Buttitta P, Cammarata M, Lo Presti A, Maresi E, Zumpani L, Giuffrè L.
    Am J Med Genet; 1990 Oct 15; 37(2):244-9. PubMed ID: 2147361
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  • 18. [Intrauterine diagnosis of holoprosencephaly].
    Bonilla-Musoles F, Ramirez JV, Pérez-Gil M, Pellicer A.
    Ultraschall Med; 1984 Feb 15; 5(1):24-8. PubMed ID: 6710120
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  • 19. The obstetric significance of holoprosencephaly.
    Chervenak FA, Isaacson G, Mahoney MJ, Tortora M, Mesologites T, Hobbins JC.
    Obstet Gynecol; 1984 Jan 15; 63(1):115-21. PubMed ID: 6691008
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  • 20. Further delineation of the dup(3q) syndrome.
    Wilson GN, Dasouki M, Barr M.
    Am J Med Genet; 1985 Sep 15; 22(1):117-23. PubMed ID: 4050847
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