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


86 related items for PubMed ID: 7093017

  • 1. [Holt syndrome: an autosomal dominant, heterogeneous, acral malformation].
    Hernández Téllez A, Corona Rivera E, Martínez-Basalo C, Nazará Cazorla Z, Aguirre-Negrete MG, Cantú JM.
    Bol Med Hosp Infant Mex; 1982 Feb; 39(2):131-3. PubMed ID: 7093017
    [No Abstract] [Full Text] [Related]

  • 2. [Stapes ankylosis as a symptom of autosomal dominant symphalangia].
    Theunissen EJ, Cremers CW.
    Ned Tijdschr Geneeskd; 1984 Apr 14; 128(15):712-4. PubMed ID: 6717641
    [No Abstract] [Full Text] [Related]

  • 3. Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes.
    Robin NH, Segel B, Carpenter G, Muenke M.
    Am J Med Genet; 1996 Mar 15; 62(2):184-91. PubMed ID: 8882401
    [Abstract] [Full Text] [Related]

  • 4. Holt-Oram syndrome: postaxial and central polydactyly as variable manifestations in a four generations family.
    Moens P, De Smet L, Fabry G, Fryns JP.
    Genet Couns; 1993 Mar 15; 4(4):277-80. PubMed ID: 8110414
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar 15; 14(2):91-2. PubMed ID: 8469651
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Heritable nail disorders.
    Kucirka SJ, Scher RK.
    Dermatol Clin; 1987 Jan 15; 5(1):179-91. PubMed ID: 3030593
    [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. Relatively high prevalence of the Meckel syndrome among Jews.
    Fried K.
    Isr J Med Sci; 1973 Jan 15; 9(9):1399. PubMed ID: 4775123
    [No Abstract] [Full Text] [Related]

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

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

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 19. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 Jan 15; 6(4):309-12. PubMed ID: 8775417
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 5.