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

152 related items for PubMed ID: 8669452

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Characteristic facial dysmorphism, arachnodactyly and mental retardation: another case.
    Van Buggenhout GJ, Akkermans-Scholten AC, Hamel BC.
    Genet Couns; 1995; 6(1):61-3. PubMed ID: 7794564
    [No Abstract] [Full Text] [Related]

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

  • 5. Additional case of craniofacial and digital anomalies as reported by Harrod et al.
    Jurenka SB, Van Allen MI.
    Am J Med Genet; 1996 Jan 11; 61(2):168-70. PubMed ID: 8669446
    [Abstract] [Full Text] [Related]

  • 6. [Rubinstein-Taybi syndrome. Apropos of 2 new cases].
    Legrand J, Maurat JC.
    Arch Ophtalmol Rev Gen Ophtalmol; 1973 Oct 11; 33(10):641-60. PubMed ID: 4151444
    [No Abstract] [Full Text] [Related]

  • 7. Two cases of Townes-Brocks syndrome.
    Doray B, Langer B, Stoll C.
    Genet Couns; 1999 Oct 11; 10(4):359-67. PubMed ID: 10631923
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Kabuki make-up (Niikawa-Kuroki) syndrome in a girl presenting with vitiligo vulgaris, cleft palate, somatic and psychomotor retardation and facial dysmorphism.
    Schrander-Stumpel C, Theunissen P, Hulsmans R, Fryns JP.
    Genet Couns; 1993 Oct 11; 4(1):71-2. PubMed ID: 8471227
    [No Abstract] [Full Text] [Related]

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

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

  • 12. Megadolichosigmoid in a young male with Aarskog syndrome.
    Casteels M, Samain H, Penninckx F, Coremans G, Beirinckx J, Fryns JP.
    Genet Couns; 1994 Oct 11; 5(1):81-3. PubMed ID: 8031541
    [No Abstract] [Full Text] [Related]

  • 13. Townes-Brocks syndrome in two mentally retarded youngsters.
    Cameron TH, Lachiewicz AM, Aylsworth AS.
    Am J Med Genet; 1991 Oct 01; 41(1):1-4. PubMed ID: 1951448
    [Abstract] [Full Text] [Related]

  • 14. [Anus-hand-ear syndrome (Townes-Brocks syndrome)].
    Kurosawa K.
    Ryoikibetsu Shokogun Shirizu; 2001 Oct 01; (33):211-2. PubMed ID: 11462405
    [No Abstract] [Full Text] [Related]

  • 15. Phenotypic variability in Townes-Brocks syndrome.
    Monteiro de Pina-Neto J.
    Am J Med Genet; 1984 May 01; 18(1):147-52. PubMed ID: 6741990
    [Abstract] [Full Text] [Related]

  • 16. [Townes-Brocks syndrome].
    Ishikiriyama S.
    Ryoikibetsu Shokogun Shirizu; 1996 May 01; (15):305-6. PubMed ID: 9048024
    [No Abstract] [Full Text] [Related]

  • 17. [Cohen syndrome: report of two cases in female twins].
    Arcas Martínez J, García Peñas JJ, Ramos Lizana J, Díaz González C, Pascual Castroviejo I.
    An Esp Pediatr; 1991 Jan 01; 34(1):83-5. PubMed ID: 2018266
    [No Abstract] [Full Text] [Related]

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

  • 19. [Molecular diagnosis of CHARGE syndrom].
    Pedersen AM, Skovby F.
    Ugeskr Laeger; 2007 Jan 29; 169(5):402-6. PubMed ID: 17280632
    [Abstract] [Full Text] [Related]

  • 20. Complicated anophthalmos.
    Bajwa GS, Thapar K, Dhawan AK, Kapoor A.
    Indian Pediatr; 1995 Apr 29; 32(4):480-2. PubMed ID: 8635814
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.