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Journal Abstract Search

181 related items for PubMed ID: 8677114

  • 1. Monosomy 7 syndrome associated with congenital adrenal hypoplasia and male pseudohermaphroditism.
    Le SQ, Kutteh WH.
    Obstet Gynecol; 1996 May; 87(5 Pt 2):854-6. PubMed ID: 8677114
    [Abstract] [Full Text] [Related]

  • 2. [Causes of ambiguous external genitalia in neonates].
    Zdravković D, Milenković T, Sedlecki K, Guć-Sćekić M, Rajić V, Banićević M.
    Srp Arh Celok Lek; 2001 May; 129(3-4):57-60. PubMed ID: 11534268
    [Abstract] [Full Text] [Related]

  • 3. [Effect of prepuberal gonadectomy in partial androgen resistance syndrome].
    Garcia Morales MA, Barron Vallejo J, Limon Luque L.
    Ginecol Obstet Mex; 1996 Mar; 64():120-1. PubMed ID: 8729188
    [Abstract] [Full Text] [Related]

  • 4. Instability of chromosome 7 in colony forming cells of patients with aplastic anemia.
    Ueda H, Tashiro S, Kojima S, Tanaka K, Eguchi M, Ueda K, Kamada N.
    Int J Hematol; 1999 Jul; 70(1):13-9. PubMed ID: 10446489
    [Abstract] [Full Text] [Related]

  • 5. Abnormalities of human autosomes. I. Ambigous genitalia associated with a translocation 46,XY, t(Cq+;Cq-).
    German J, Simpson JL.
    Birth Defects Orig Artic Ser; 1971 May; 7(6):145-9. PubMed ID: 5173157
    [Abstract] [Full Text] [Related]

  • 6. Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndrome.
    Reardon W, Gibbons RJ, Winter RM, Baraitser M.
    Am J Med Genet; 1995 Jan 30; 55(3):285-7. PubMed ID: 7726224
    [Abstract] [Full Text] [Related]

  • 7. [Myelodysplastic syndrome developed in a mother and her son whose bone marrow karyotype showed monosomy 7].
    Wakita A, Komatsu H, Banno S, Ando M, Nitta M, Takada K, Mitomo Y, Ueda R.
    Rinsho Ketsueki; 1996 Apr 30; 37(4):311-6. PubMed ID: 8847801
    [Abstract] [Full Text] [Related]

  • 8. X-linked congenital adrenal hypoplasia: proposal pathogenesis.
    Preeyasombat C, Sriphrapradang A, Chaubtam L.
    J Med Assoc Thai; 1989 Jan 30; 72 Suppl 1():164-73. PubMed ID: 2732638
    [Abstract] [Full Text] [Related]

  • 9. [Monosomy r(13). Report of a new case].
    Cuadrado Martín M, Boldova Aguar C, Carrasco Lorente S, Martínez Laborda S, López-Pisón J, Baldellou Vázquez A, Labarta Aizpún J, Marco Tello A, Rebage Moisés V.
    An Esp Pediatr; 2000 Dec 30; 53(6):592-5. PubMed ID: 11148159
    [Abstract] [Full Text] [Related]

  • 10. [A case of male pseudohermaphroditism with structural abnormalities of Y chromosome (ring Y)].
    Watanabe H, Hachisuka Y, Watase H, Fushimi N, Ohtaguro K.
    Hinyokika Kiyo; 1988 Aug 30; 34(8):1469-74. PubMed ID: 3057830
    [Abstract] [Full Text] [Related]

  • 11. Myelodysplastic syndrome associated with monosomy 7 in childhood: a retrospective study.
    Aktas D, Tuncbilek E.
    Cancer Genet Cytogenet; 2006 Nov 30; 171(1):72-5. PubMed ID: 17074595
    [Abstract] [Full Text] [Related]

  • 12. Low-level mosaicism for both trisomy 15 and monosomy-X in amniotic fluid cells confirmed in fetal tissues.
    Hansson K, Poelma WM, Zondervan HA, Leschot NJ.
    Prenat Diagn; 1998 Sep 30; 18(9):975-8. PubMed ID: 9793985
    [Abstract] [Full Text] [Related]

  • 13. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J, Chernos J, Roland B.
    Am J Med Genet; 1997 Dec 19; 73(3):327-9. PubMed ID: 9415693
    [Abstract] [Full Text] [Related]

  • 14. A clinico-genetic investigation of Leydig cell hypoplasia.
    Saldanha PH, Arnhold IJ, Mendonça BB, Bloise W, Toledo SP.
    Am J Med Genet; 1987 Feb 19; 26(2):337-44. PubMed ID: 3812586
    [Abstract] [Full Text] [Related]

  • 15. Characterization of a derivative chromosome 17 by fish-technique.
    Ramesh KH, Shah HO, Sherman J, Lin JH, Verma RS.
    Ann Genet; 1996 Feb 19; 39(3):177-80. PubMed ID: 8839891
    [Abstract] [Full Text] [Related]

  • 16. Correlation between CD34 expression and chromosomal abnormalities but not clinical outcome in acute myeloid leukemia.
    Fruchart C, Lenormand B, Bastard C, Boulet D, Lesesve JF, Callat MP, Stamatoullas A, Monconduit M, Tilly H.
    Am J Hematol; 1996 Nov 19; 53(3):175-80. PubMed ID: 8895688
    [Abstract] [Full Text] [Related]

  • 17. Female pseudohermaphroditism in a fetus with a deletion 9(q22.2q31.1).
    L'Herminé AC, Aboura A, Simon-Bouy B, Robin F, Audibert F, Strouk N, Capron F, Frydman R, Tachdjian G.
    Prenat Diagn; 2002 Aug 19; 22(8):652-5. PubMed ID: 12210571
    [Abstract] [Full Text] [Related]

  • 18. Micropenis and congenital adrenal hypoplasia.
    Bourgeois MJ, Jones B, Waagner DC, Dunn D.
    Am J Perinatol; 1989 Jan 19; 6(1):69-71. PubMed ID: 2910322
    [Abstract] [Full Text] [Related]

  • 19. [Male pseudohermaphroditism. Management of etiological diagnosis. 1st part].
    Vague J, Guidon J.
    Sem Hop; 1977 Oct 23; 53(36):1915-20. PubMed ID: 208157
    [No Abstract] [Full Text] [Related]

  • 20. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
    Grammatico P, Majore S, Marrocco G, Poscente M, Mordenti C, Grammatico B, Del Porto G.
    Genet Couns; 1999 Oct 23; 10(4):351-8. PubMed ID: 10631922
    [Abstract] [Full Text] [Related]

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