These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

68 related items for PubMed ID: 3429997

  • 1. [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]

  • 2. 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]

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

  • 4. 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]

  • 5. 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]

  • 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. [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]

  • 8. 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 03; 7(6):215-28. PubMed ID: 5173165
    [Abstract] [Full Text] [Related]

  • 9. A rare cause for primary amenorrhoea.
    Ameen KH, Pinninti R.
    J Hum Reprod Sci; 2012 May 03; 5(2):218-20. PubMed ID: 23162364
    [Abstract] [Full Text] [Related]

  • 10. Recessive gonadal dysgenesis.
    Smith A.
    Clin Genet; 1983 Jan 03; 23(1):80. PubMed ID: 6831767
    [No 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 03; 39(4):318-20. PubMed ID: 8040851
    [Abstract] [Full Text] [Related]

  • 12. 46,XX gonadal dysgenesis associated with congenital nerve deafness.
    Granat M, Reiter A, Dar H, Sharf M.
    Int J Gynaecol Obstet; 1979 Apr 03; 17(3):231-3. PubMed ID: 42575
    [Abstract] [Full Text] [Related]

  • 13. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome.
    Miny P, Lenz W.
    Am J Med Genet; 1985 Jun 03; 21(2):317-24. PubMed ID: 4014313
    [Abstract] [Full Text] [Related]

  • 14. A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.
    Jain PK, Lalwani AK, Li XC, Singleton TL, Smith TN, Chen A, Deshmukh D, Verma IC, Smith RJ, Wilcox ER.
    Genomics; 1998 Jun 01; 50(2):290-2. PubMed ID: 9653658
    [Abstract] [Full Text] [Related]

  • 15. Familial 46,XX gonadal dysgenesis.
    Portuondo JA, Neyro JL, Benito JA, de los Rios A, Barral A.
    Int J Fertil; 1987 Jun 01; 32(1):56-8. PubMed ID: 2880817
    [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 01; 20(5):305-8. PubMed ID: 17868898
    [Abstract] [Full Text] [Related]

  • 17. [A familial XY gonadal dysgenesis causing high incidence of embryonic gonadal tumors- a report of the fourth dysgerminoma in sibling suffering from 46, XY gonadal dysgenesis (author's transl)].
    E Z, Xu XL, Li C, Gao FZ.
    Zhonghua Zhong Liu Za Zhi; 1981 May 01; 3(2):89-90. PubMed ID: 7307902
    [No Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Gonadal dysgenesis in del(18p) syndrome.
    Telvi L, Bernheim A, Ion A, Fouquet F, Le Bouc Y, Chaussain JL.
    Am J Med Genet; 1995 Jul 17; 57(4):598-600. PubMed ID: 7573136
    [Abstract] [Full Text] [Related]

  • 20. [Study on familial 46, XY gonadal dysgenesis and high risk of gonadal tumors. III. Establishment of a fibroblast cell line (TGD-8F) on individual with 46, XY gonadal dysgenesis].
    E Z.
    Zhonghua Zhong Liu Za Zhi; 1983 Jan 17; 5(1):29-30. PubMed ID: 6851828
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 4.