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Journal Abstract Search

109 related items for PubMed ID: 6650568

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

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

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

  • 4. [Perrault's syndrome: familial gonadal dysgenesis with sensorineural deafness].
    Yoshida K, Takashima M, Otsuka H, Okamura Y, Hirano T, Matsuzaki H.
    Nihon Sanka Fujinka Gakkai Zasshi; 1987 Dec; 39(12):2217-20. PubMed ID: 3429997
    [No Abstract] [Full Text] [Related]

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

  • 6. [Perrault's syndrome: two cases].
    Bellassoued M, Mnif M, Marouene H, Kammoun S, Ghorbel A, Mnif J, Ayadi F, Drira M, Kchaou MS, Abid M.
    Ann Endocrinol (Paris); 2001 Dec; 62(6):534-7. PubMed ID: 11845030
    [Abstract] [Full Text] [Related]

  • 7. 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]

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

  • 9. Perrault syndrome with Marfanoid habitus in two siblings.
    Jacob JJ, Paul TV, Mathews SS, Thomas N.
    J Pediatr Adolesc Gynecol; 2007 Oct 28; 20(5):305-8. PubMed ID: 17868898
    [Abstract] [Full Text] [Related]

  • 10. Autosomal recessive malformation syndrome with minor manifestation in the heterozygotes: a preliminary report of a possible new syndrome.
    Paes-Alves AF, Azevêdo ES, Sousa MG, Almeida-Melo N, Oliveira-Filho OJ.
    Am J Med Genet; 1991 Nov 01; 41(2):141-52. PubMed ID: 1785624
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 39(4):318-20. PubMed ID: 8040851
    [Abstract] [Full Text] [Related]

  • 12. Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?
    Moog U, Bleeker-Wagemakers EM, Crobach P, Vles JS, Schrander-Stumpel CT.
    Am J Med Genet; 1998 Jul 07; 78(3):263-6. PubMed ID: 9677063
    [Abstract] [Full Text] [Related]

  • 13. Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance.
    Koiffmann CP, Wajntal A, Huyke BJ, Castro RM.
    Am J Med Genet; 1988 Feb 07; 29(2):263-8. PubMed ID: 3354597
    [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. Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene.
    Mendonça BB, Barbosa AS, Arnhold IJ, McElreavey K, Fellous M, Moreira-Filho CA.
    Am J Med Genet; 1994 Aug 01; 52(1):39-43. PubMed ID: 7977459
    [Abstract] [Full Text] [Related]

  • 16. XX-agonadism in a fetus with multiple dysraphic lesions: a new syndrome.
    Kennerknecht I, Mattfeldt T, Paulus W, Nitsch C, Negri G, Barbi G, Just W, Schwemmle S, Vogel W.
    Am J Med Genet; 1997 Jun 27; 70(4):413-4. PubMed ID: 9182784
    [Abstract] [Full Text] [Related]

  • 17. Agonadism in two sisters with XY gonosomal constitution, mental retardation, short stature, severely retarded bone age, and multiple extragenital malformations: a new autosomal recessive syndrome.
    Kennerknecht I, von Saurma P, Brenner R, Just W, Barbi G, Sorgo W, Heinze E, Wolf AS, Schneider V, Günther KP.
    Am J Med Genet; 1995 Oct 23; 59(1):62-7. PubMed ID: 8849014
    [Abstract] [Full Text] [Related]

  • 18. A rare cause for primary amenorrhoea.
    Ameen KH, Pinninti R.
    J Hum Reprod Sci; 2012 May 23; 5(2):218-20. PubMed ID: 23162364
    [Abstract] [Full Text] [Related]

  • 19. 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 23; 7(6):215-28. PubMed ID: 5173165
    [Abstract] [Full Text] [Related]

  • 20. Familial ovarian dysgenesis in 46,XX females.
    Vesely DL, Bower RH, Kohler PO, Char F.
    Am J Med Sci; 1980 May 23; 280(3):157-66. PubMed ID: 6779629
    [Abstract] [Full Text] [Related]

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