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Journal Abstract Search

198 related items for PubMed ID: 8826428

  • 1. Gonadal (ovarian) dysgenesis in 46,XX individuals: frequency of the autosomal recessive form.
    Meyers CM, Boughman JA, Rivas M, Wilroy RS, Simpson JL.
    Am J Med Genet; 1996 Jun 28; 63(4):518-24. PubMed ID: 8826428
    [Abstract] [Full Text] [Related]

  • 2. Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data.
    Simpson JL, Christakos AC, Horwith M, Silverman FS.
    Birth Defects Orig Artic Ser; 1971 May 28; 7(6):215-28. PubMed ID: 5173165
    [Abstract] [Full Text] [Related]

  • 3. The Perrault syndrome: autosomal recessive ovarian dysgenesis with facultative, non-sex-limited sensorineural deafness.
    Pallister PD, Opitz JM.
    Am J Med Genet; 1979 May 28; 4(3):239-46. PubMed ID: 517579
    [Abstract] [Full Text] [Related]

  • 4. The Perrault syndrome: clinical report and review.
    Nishi Y, Hamamoto K, Kajiyama M, Kawamura I.
    Am J Med Genet; 1988 Nov 28; 31(3):623-9. PubMed ID: 3067578
    [Abstract] [Full Text] [Related]

  • 5. Left ovarian cyst and right streak ovary in a neonate with a normal karyotype. Report of a case of neonatal Slotnick-Goldfarb syndrome or recessive gonadal dysgenesis.
    Freud E, Zer M, Merlob P.
    J Reprod Med; 1994 Apr 28; 39(4):318-20. PubMed ID: 8040851
    [Abstract] [Full Text] [Related]

  • 6. Perrault's syndrome in two sisters.
    Bösze P, Skripeczky K, Gaál M, Tóth A, László J.
    Am J Med Genet; 1983 Oct 28; 16(2):237-41. PubMed ID: 6650568
    [Abstract] [Full Text] [Related]

  • 7. Sensorineural hearing loss associated to gonadal dysgenesis in sisters: Perrault's syndrome.
    Cruz OL, Pedalini ME, Caropreso CA.
    Am J Otol; 1992 Jan 28; 13(1):82-3. PubMed ID: 1598993
    [Abstract] [Full Text] [Related]

  • 8. Familial dysgerminoma associated with 46, XX pure gonadal dysgenesis.
    Namavar-Jahromi B, Mohit M, Kumar PV.
    Saudi Med J; 2005 May 28; 26(5):872-4. PubMed ID: 15951888
    [Abstract] [Full Text] [Related]

  • 9. Familial 46,XX gonadal dysgenesis.
    Portuondo JA, Neyro JL, Benito JA, de los Rios A, Barral A.
    Int J Fertil; 1987 May 28; 32(1):56-8. PubMed ID: 2880817
    [Abstract] [Full Text] [Related]

  • 10. Over-expression of Müllerian inhibiting substance mRNA in the Turner syndrome ovary.
    Modi D, Sane S, Bhartiya D.
    Sex Dev; 2009 May 28; 3(5):245-52. PubMed ID: 19940443
    [Abstract] [Full Text] [Related]

  • 11. Brief historical note: the concept of "gonadal dysgenesis".
    Opitz JM, Pallister PD.
    Am J Med Genet; 1979 May 28; 4(4):333-43. PubMed ID: 395846
    [Abstract] [Full Text] [Related]

  • 12. Familial ovarian dysgenesis in 46,XX females.
    Vesely DL, Bower RH, Kohler PO, Char F.
    Am J Med Sci; 1980 May 28; 280(3):157-66. PubMed ID: 6779629
    [Abstract] [Full Text] [Related]

  • 13. Sex chromosomal mosaicism in the gonads of patients with gonadal dysgenesis, but normal female or male karyotypes in lymphocytes.
    Röpke A, Pelz AF, Volleth M, Schlösser HW, Morlot S, Wieacker PF.
    Am J Obstet Gynecol; 2004 Apr 28; 190(4):1059-62. PubMed ID: 15118641
    [Abstract] [Full Text] [Related]

  • 14. [Familial streak gonad syndrome with 46,XX karyotype (pure gonadal dysgenesis)].
    Tóth A, Gaál M, Bösze P, Komora V, László J.
    Orv Hetil; 1985 Mar 03; 126(9):527-9. PubMed ID: 3991192
    [No Abstract] [Full Text] [Related]

  • 15. [Diagnostic principles of gonadal dysgenesis in adolescents].
    Chipashvili MK, Kristesashvili DI, Chopikashvili NA, Kopaliani NSh.
    Georgian Med News; 2005 Nov 03; (128):24-8. PubMed ID: 16369057
    [Abstract] [Full Text] [Related]

  • 16. Perrault syndrome with Marfanoid habitus in two siblings.
    Jacob JJ, Paul TV, Mathews SS, Thomas N.
    J Pediatr Adolesc Gynecol; 2007 Oct 03; 20(5):305-8. PubMed ID: 17868898
    [Abstract] [Full Text] [Related]

  • 17. XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription.
    Zangen D, Kaufman Y, Zeligson S, Perlberg S, Fridman H, Kanaan M, Abdulhadi-Atwan M, Abu Libdeh A, Gussow A, Kisslov I, Carmel L, Renbaum P, Levy-Lahad E.
    Am J Hum Genet; 2011 Oct 07; 89(4):572-9. PubMed ID: 21963259
    [Abstract] [Full Text] [Related]

  • 18. Aplasia of the Müllerian system: evidence for probable sex-limited autosomal dominant inheritance.
    Shokeir MH.
    Birth Defects Orig Artic Ser; 1978 Oct 07; 14(6C):147-65. PubMed ID: 728579
    [Abstract] [Full Text] [Related]

  • 19. Ovarian dysgenesis with balanced autosomal translocation.
    Tullu MS, Arora P, Parmar RC, Muranjan MN, Bharucha BA.
    J Postgrad Med; 2001 Oct 07; 47(2):113-5. PubMed ID: 11832602
    [Abstract] [Full Text] [Related]

  • 20. Alopecia universalis congenita, XY gonadal dysgenesis and laryngomalacia: a novel malformation syndrome.
    El-Shanti H, Ahmad M, Ajlouni K.
    Eur J Pediatr; 2003 Jan 07; 162(1):36-40. PubMed ID: 12486505
    [Abstract] [Full Text] [Related]

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