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

Journal Abstract Search


290 related items for PubMed ID: 7996504

  • 1. Fraser syndrome.
    Chattopadhyay A, Kher AS, Udwadia AD, Sharma SV, Bharucha BA, Nicholson AD.
    J Postgrad Med; 1993; 39(4):228-30. PubMed ID: 7996504
    [Abstract] [Full Text] [Related]

  • 2. Fraser syndrome. Cryptophthalmos syndactyly syndrome.
    Tilahun M, Kifle A, Oljira B.
    Ethiop Med J; 1990 Apr; 28(2):89-90. PubMed ID: 2163830
    [No Abstract] [Full Text] [Related]

  • 3. Recurrent Fraser syndrome.
    Kiran G, Namita G, Dheeraj S.
    Prenat Diagn; 2007 Feb; 27(2):184-5. PubMed ID: 17266165
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Fraser syndrome with bladder pseudoexstrophy.
    Daia JA.
    Saudi Med J; 2001 May; 22(5):455-6. PubMed ID: 11376391
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Intrafamilial variability in Fraser syndrome.
    Prasun P, Pradhan M, Goel H.
    Prenat Diagn; 2007 Aug; 27(8):778-82. PubMed ID: 17546704
    [Abstract] [Full Text] [Related]

  • 8. [Fraser syndrome, renal agenesis and fetal ascites].
    Pérez Aytes A, Fábregat Ferrer E, Ramos Fernández V, Uixera Marzal L, Froufe Sánchez A.
    An Esp Pediatr; 1993 Aug; 39(2):163-6. PubMed ID: 8239214
    [No Abstract] [Full Text] [Related]

  • 9. [Renal agenesis and the Fraser syndrome: 4 observations].
    Vanlieferinghen P, Francannet C, Robert E, Malpuech G, Robert JM.
    J Genet Hum; 1989 Dec; 37(4-5):373-7. PubMed ID: 2635714
    [Abstract] [Full Text] [Related]

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

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

  • 12. Waardenburg syndrome: a report of three cases.
    Ghosh SK, Bandyopadhyay D, Ghosh A, Biswas SK, Mandal RK.
    Indian J Dermatol Venereol Leprol; 2010 Dec; 76(5):550-2. PubMed ID: 20826997
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review.
    Bastaki L, El-Nabi MM, Azab AS, Gouda SA, Al-Wadaani AM, Naguib KK.
    East Mediterr Health J; 2007 Dec; 13(4):975-9. PubMed ID: 17955782
    [No Abstract] [Full Text] [Related]

  • 15. Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the father.
    Ioan DM, Dagomiz D, Fryns JP.
    Genet Couns; 2002 Dec; 13(2):187-9. PubMed ID: 12150221
    [Abstract] [Full Text] [Related]

  • 16. Prenatal death in Fraser syndrome.
    Comstock JM, Putnam AR, Opitz JM, Pysher TJ, Szakacs J.
    Fetal Pediatr Pathol; 2005 Dec; 24(4-5):223-38. PubMed ID: 16396829
    [Abstract] [Full Text] [Related]

  • 17. Sandrow syndrome of mirror hands and feet and facial abnormalities.
    Kogekar N, Teebi AS, Vockley J.
    Am J Med Genet; 1993 Apr 15; 46(2):126-8. PubMed ID: 8387243
    [Abstract] [Full Text] [Related]

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

  • 19. Evidence for genetic anticipation in the oculodentodigital syndrome.
    Shapiro RE, Griffin JW, Stine OC.
    Am J Med Genet; 1997 Jul 11; 71(1):36-41. PubMed ID: 9215766
    [Abstract] [Full Text] [Related]

  • 20. [Oculodentodigital dysplasia: genetic counselling, reproductive expectatives and molecular assay of a clinical case referred to preimplantational diagnosis].
    Martínez-García M, Bustamante-Aragonés A, Lorda I, Trujillo-Tiebas MJ.
    Med Clin (Barc); 2012 May 12; 138(13):592-3. PubMed ID: 22024562
    [No Abstract] [Full Text] [Related]


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