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Journal Abstract Search

157 related items for PubMed ID: 3953673

  • 1. Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata.
    Wertelecki W, Breg WR, Graham JM, Iinuma K, Puck SM, Sergovich FR.
    Am J Med Genet; 1986 Mar; 23(3):739-49. PubMed ID: 3953673
    [Abstract] [Full Text] [Related]

  • 2. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
    Crowe CA, Schwartz S, Black CJ, Jaswaney V.
    Am J Med Genet; 1997 Sep 05; 71(4):406-13. PubMed ID: 9286446
    [Abstract] [Full Text] [Related]

  • 3. Mosaic double aneuploidy (45,X/47,XX,+8) with aortic dissection.
    Lee MN, Choi KH, Kim DK, Kim SH.
    Genet Couns; 2014 Sep 05; 25(2):177-82. PubMed ID: 25059016
    [Abstract] [Full Text] [Related]

  • 4. Ullrich-Turner syndrome in monozygotic twins.
    Al-Awadi SA, Cuschieri A, Farag TI, Naguib K, Teebi AS, Al-Othman SA, Bahig AH.
    Am J Med Genet; 1983 Aug 05; 15(4):537-42. PubMed ID: 6684396
    [Abstract] [Full Text] [Related]

  • 5. Brief clinical report: del(X) (q26) in a phenotypically normal woman and her daughter who also has trisomy 21.
    Taysi K.
    Am J Med Genet; 1983 Feb 05; 14(2):367-72. PubMed ID: 6188379
    [Abstract] [Full Text] [Related]

  • 6. Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
    Karadima G, Bugge M, Nicolaidis P, Vassilopoulos D, Avramopoulos D, Grigoriadou M, Albrecht B, Passarge E, Annerén G, Blennow E, Clausen N, Galla-Voumvouraki A, Tsezou A, Kitsiou-Tzeli S, Hahnemann JM, Hertz JM, Houge G, Kuklík M, Macek M, Lacombe D, Miller K, Moncla A, López Pajares I, Patsalis PC, Petersen MB.
    Eur J Hum Genet; 1998 Feb 05; 6(5):432-8. PubMed ID: 9801867
    [Abstract] [Full Text] [Related]

  • 7. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
    González-del-Angel A, Blanco B, del Castillo V, Carnevale A.
    Rev Invest Clin; 1995 Feb 05; 47(2):117-25. PubMed ID: 7610280
    [Abstract] [Full Text] [Related]

  • 8. [45,X/46,X,del(Yq) sex chromosome mosaicism--analysis of the phenotypic expression].
    Werner W, John B, Tuschy U, Knorr B, Herrmann FH.
    Zentralbl Gynakol; 1985 Feb 05; 107(5):265-79. PubMed ID: 3993267
    [Abstract] [Full Text] [Related]

  • 9. Ullrich-Turner phenotype with unusual manifestation in a patient with mosaicism 45,X/47,XX,+18.
    Franceschini P, Guala A, Camerano P, Franceschini D, Vardeu MP, Signorile F.
    Am J Med Genet; 1996 Mar 01; 62(1):26-8. PubMed ID: 8779320
    [Abstract] [Full Text] [Related]

  • 10. Ullrich-Turner syndrome and neurofibromatosis-1.
    Schorry EK, Lovell AM, Milatovich A, Saal HM.
    Am J Med Genet; 1996 Dec 30; 66(4):423-5. PubMed ID: 8989459
    [Abstract] [Full Text] [Related]

  • 11. [Extreme tissue mosaicism in trisomy 8 syndrome. Trisomy 8 in fibroblasts and normal karyotype in lymphocytes].
    Meisel-Stosiek M, Pfeiffer RA, Tietze HU.
    Klin Padiatr; 1983 Dec 30; 195(5):365-8. PubMed ID: 6632718
    [Abstract] [Full Text] [Related]

  • 12. Variable clinical expression of mosaic trisomy 16 in the newborn infant.
    Devi AS, Velinov M, Kamath MV, Eisenfeld L, Neu R, Ciarleglio L, Greenstein R, Benn P.
    Am J Med Genet; 1993 Aug 15; 47(2):294-8. PubMed ID: 8213923
    [Abstract] [Full Text] [Related]

  • 13. [Down's syndrome with confirmation of trisomy G solely in fibroblast cultures].
    Haberlandt W.
    J Genet Hum; 1973 Sep 15; 21(3):215-22. PubMed ID: 4282491
    [No Abstract] [Full Text] [Related]

  • 14. Ullrich-Turner syndrome in an XY female fetus with deletion of the sex-determining portion of the Y chromosome.
    Blagowidow N, Page DC, Huff D, Mennuti MT.
    Am J Med Genet; 1989 Oct 15; 34(2):159-62. PubMed ID: 2816992
    [Abstract] [Full Text] [Related]

  • 15. Trisomy 12/monosomy X/normal female mosaicism: prenatal detection and confirmation in a liveborn.
    Spiro R, Rita D, Jazmines L, Jones C, Booth CW.
    Prenat Diagn; 1996 Aug 15; 16(8):734-40. PubMed ID: 8878284
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  • 17. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
    Gentile M, Buonadonna AL, Cariola F, Fiorente P, Valenzano MC, Guanti G.
    J Med Genet; 1999 Jan 15; 36(1):77-82. PubMed ID: 9950374
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  • 20. Monozygotic twins discordant for Ullrich-Turner syndrome.
    Weiss E, Loevy H, Saunders A, Pruzansky S, Rosenthal IM.
    Am J Med Genet; 1982 Dec 15; 13(4):389-99. PubMed ID: 6891562
    [Abstract] [Full Text] [Related]

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