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

284 related items for PubMed ID: 8040851

  • 1. 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; 39(4):318-20. PubMed ID: 8040851
    [Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. The streak gonad syndrome.
    Bösze P, László J.
    Obstet Gynecol; 1979 Nov 03; 54(5):544-8. PubMed ID: 503377
    [Abstract] [Full Text] [Related]

  • 4. Ovarian dysgenesis with balanced autosomal translocation.
    Tullu MS, Arora P, Parmar RC, Muranjan MN, Bharucha BA.
    J Postgrad Med; 2001 Nov 03; 47(2):113-5. PubMed ID: 11832602
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. 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]

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

  • 8. 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]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Gonadal dysgenesis and Rokitansky syndrome. A case report.
    Güitrón-Cantú A, López-Vera E, Forsbach-Sánchez G, Leal-Garza CH, Cortés-Gutiérrez EI, González-Pico I.
    J Reprod Med; 1999 Oct 28; 44(10):891-3. PubMed ID: 10554753
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. [Rudimentary ovary syndrome].
    Bösze P, Kovács Z, László J.
    Orv Hetil; 1990 Jan 14; 131(2):75-8. PubMed ID: 2296462
    [Abstract] [Full Text] [Related]

  • 16. [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 Jan 14; 129(3-4):57-60. PubMed ID: 11534268
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Perrault's syndrome in two sisters.
    Bösze P, Skripeczky K, Gaál M, Tóth A, László J.
    Am J Med Genet; 1983 Oct 14; 16(2):237-41. PubMed ID: 6650568
    [Abstract] [Full Text] [Related]

  • 20. An infant with a mosaic 45,X/46,X,psu dic(Y) (pter-->q11.2::q11.2-->pter) karyotype and mixed gonadal dysgenesis studied for extent of mosaicism in the gonads.
    Reddy KS, Sulcova V, Ho CK, Conner ED, Khurana A.
    Am J Med Genet; 1996 Dec 30; 66(4):441-4. PubMed ID: 8989464
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.