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

207 related items for PubMed ID: 11423730

  • 1. [Roberts-SC phocomelia syndrome].
    Musfeld DA, Bühler EM, Heinzl S.
    Gynakol Geburtshilfliche Rundsch; 2001; 41(1):3-7. PubMed ID: 11423730
    [Abstract] [Full Text] [Related]

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

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

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

  • 7. [Roberts-SC phocomelia syndrome].
    Kawame H.
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):234-5. PubMed ID: 11057210
    [No Abstract] [Full Text] [Related]

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

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

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

  • 11. [Genetic morphological fatal syndromes. The Fryns syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar; 14(2):92-3. PubMed ID: 8469652
    [No Abstract] [Full Text] [Related]

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

  • 13. Roberts-SC phocomelia syndrome with exencephaly.
    Verloes A, Herens C, Van Maldergem L, Retz MC, Dodinval P.
    Ann Genet; 1989 Mar; 32(3):169-70. PubMed ID: 2817778
    [Abstract] [Full Text] [Related]

  • 14. [Meckel-Gruber syndrome].
    Flessa A, Rempen A, Schmausser B, Marx A.
    Z Geburtshilfe Neonatol; 1996 Mar; 200(2):66-8. PubMed ID: 8767290
    [Abstract] [Full Text] [Related]

  • 15. Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation.
    Schüle B, Oviedo A, Johnston K, Pai S, Francke U.
    Am J Hum Genet; 2005 Dec; 77(6):1117-28. PubMed ID: 16380922
    [Abstract] [Full Text] [Related]

  • 16. Roberts-SC phocomelia syndrome: a case with additional anomalies.
    Satar M, Atici A, Bişak U, Tunali N.
    Clin Genet; 1994 Feb; 45(2):107-8. PubMed ID: 8004795
    [Abstract] [Full Text] [Related]

  • 17. A sibship with Roberts/SC phocomelia syndrome.
    Holmes-Siedle M, Seres-Santamaria A, Crocker M, Hall JG, Crouchman M.
    Am J Med Genet; 1990 Sep; 37(1):18-22. PubMed ID: 2240038
    [Abstract] [Full Text] [Related]

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

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Phocomelia, ectrodactyly, skull defect and urinary system anomaly: Schinzel-phocomelia syndrome?
    Evliyaoğlu N, Temoçin AK, Altintaş DU, Duman N, Satar N, Süleymanova D.
    Clin Genet; 1996 Feb; 49(2):70-3. PubMed ID: 8740915
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.