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Journal Abstract Search

109 related items for PubMed ID: 8177840

  • 1. 45,X/46,XX/47,XXX phenotype.
    Lebel RR, Elejalde BR, de Elejalde MM, Avila T.
    Prenat Diagn; 1993 Dec; 13(12):1165-6. PubMed ID: 8177840
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  • 3. Fetoscopy and fetal blood sampling in the management of a twin pregnancy with 45,X/46,XX amniotic fluid cell mosaicism and a suspected fluid sampling error.
    Garrett C, Blunt S, Daker MG, Sharp J, Rodeck CH.
    Prenat Diagn; 1983 Dec; 3(2):165-8. PubMed ID: 6622397
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  • 4. Prenatal diagnosis and gonadal findings in X/XXX mosaicism.
    Kohn G, Cohen MM, Beyth Y, Ornoy A.
    J Med Genet; 1977 Apr; 14(2):120-3. PubMed ID: 856232
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  • 8. SRY-negative XX fetus with complete male phenotype.
    Vilain E, Le Fiblec B, Morichon-Delvallez N, Brauner R, Dommergues M, Dumez Y, Jaubert F, Boucekkine C, McElreavey K, Vekemans M.
    Lancet; 1994 Jan 22; 343(8891):240-1. PubMed ID: 7904700
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  • 11. XX/XY chimerism encountered during prenatal diagnosis.
    Freiberg AS, Blumberg B, Lawce H, Mann J.
    Prenat Diagn; 1988 Jul 22; 8(6):423-6. PubMed ID: 3211844
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  • 12. Prenatal diagnosis of 45,X/46,XX.
    Hsu LY.
    Am J Hum Genet; 1996 Mar 22; 58(3):634-6. PubMed ID: 8644723
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  • 13. Prenatal diagnosis of 45,X/46,XX mosaicism and 45,X: implications for postnatal outcome.
    Koeberl DD, McGillivray B, Sybert VP.
    Am J Hum Genet; 1995 Sep 22; 57(3):661-6. PubMed ID: 7668295
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  • 14. Maternal sex chromosome mosaicism diagnosed by amniocentesis and percutaneous umbilical cord sampling.
    Hunter AG, D'Alton M, Ivey B, Wang HS, Thompson DW.
    Prenat Diagn; 1988 Nov 22; 8(9):673-5. PubMed ID: 3211856
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  • 17. [Prenatal cytogenetic diagnosis of a 69,XXX/46,XX fetus].
    Doria Lamba Carbone L, Pierluigi M, Ferro MA.
    Pathologica; 1985 Nov 22; 77(1052):761-6. PubMed ID: 3842997
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