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Journal Abstract Search

134 related items for PubMed ID: 6829387

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  • 25. Prenatal genetic counseling.
    Jackson LG.
    Prim Care; 1976 Dec; 3(4):701-16. PubMed ID: 1051521
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  • 27. Prenatal diagnosis of a large heteromorphic region in a chromosome 5: implications for genetic counseling.
    Fineman RM, Issa B, Weinblatt V.
    Am J Med Genet; 1989 Apr; 32(4):498-9. PubMed ID: 2773992
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  • 28. [Prenatal diagnosis of the cri-du-chat syndrome in the case of balanced 5p--; 18p+ translocation in the mother].
    Zolotukhina TV, Butomo IV, Rozovskiĭ IS, Grinberg KN.
    Genetika; 1981 Apr; 17(7):1304-8. PubMed ID: 7196856
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  • 29. Prenatal diagnosis of mosaicism identified in amniotic fluid cell cultures.
    Sahin FI, Yilmaz Z, Uckuyu A, Ozalp O, Tarim E, Deren O, Yanik F.
    Genet Couns; 2006 Apr; 17(3):341-8. PubMed ID: 17100203
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  • 34. Diagnosis of a triploid fetus at genetic amniocentesis.
    Porreco RP, Matson MR, Young PE, Bradshaw C, Leopold G, Jones OW.
    Obstet Gynecol; 1980 Jul; 56(1):115-8. PubMed ID: 7383475
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  • 35. High resolution chromosome analysis and in situ hybridization on amniotic fluid for diagnosis of a cryptic translocation.
    Guichet A, Briault S, Moraine C.
    Prenat Diagn; 1998 Apr; 18(4):399-403. PubMed ID: 9602490
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  • 36. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].
    Steinborn A, Röddiger S, Born HJ, Baier P, Halberstadt E.
    Z Geburtshilfe Neonatol; 1996 Apr; 200(5):186-90. PubMed ID: 9035828
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  • 37. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP, Devriendt K, Chern SR, Lee CC, Wang W, Lin SP.
    Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
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  • 38. [The problem of sex chromosome aneuploidy in genetic counseling using amniocentesis].
    Engel E, Engel-De Montmollin M, Delozier C.
    J Genet Hum; 1980 Sep; 28(3):257-66. PubMed ID: 7463026
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  • 40. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.
    Pazarbaşi A, Demirhan O, Turgut M, Güzel I, Taştemir D.
    Genet Couns; 2008 Sep; 19(3):301-8. PubMed ID: 18990986
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