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Journal Abstract Search

237 related items for PubMed ID: 7917121

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  • 3. [Detection or exclusion of fetal trisomy 18 by in-situ-hybridization of the histologic section].
    Wille S, Mehraein Y.
    Geburtshilfe Frauenheilkd; 1993 Oct; 53(10):684-8. PubMed ID: 8270150
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  • 4. A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance.
    Fryns JP, Moerman P.
    Genet Couns; 1998 Oct; 9(1):61-2. PubMed ID: 9555592
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  • 5. Trisomy 22 confirmed by fluorescent in situ hybridization.
    Stratton RF, DuPont BR, Mattern VL, Young RS, McCourt JW, Moore CM.
    Am J Med Genet; 1993 Apr 01; 46(1):109-12. PubMed ID: 8494030
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  • 10. 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. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
    Tschernigg M, Petek E, Leonhardtsberger A, Wagner K, Kroisel PM.
    Genet Couns; 2002 Mar 01; 13(3):303-7. PubMed ID: 12416638
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  • 18. Prenatal diagnosis and characterization of an analphoid marker chromosome 16.
    Tabet AC, Gosset P, Elghezal H, Fontaine S, Martinovic J, Encha Razavi F, Romana S, Vekemans M, Morichon-Delvallez N.
    Prenat Diagn; 2004 Sep 01; 24(9):733-6. PubMed ID: 15386469
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  • 19. Detection of a subtle rearrangement of chromosome 22 using molecular techniques.
    Biesecker LG, Rosenberg M, Dziadzio L, Ledbetter DH, Ning Y, Sarneso C, Rosenbaum K.
    Am J Med Genet; 1995 Sep 25; 58(4):389-94. PubMed ID: 8533859
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  • 20. [Atypical cat eye syndrome. Fluorescence in situ hybridization of metaphase chromosomes].
    Bartsch O, Aksu F, Fenner A, Schwinger E.
    Monatsschr Kinderheilkd; 1992 Aug 25; 140(8):460-3. PubMed ID: 1359403
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