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

231 related items for PubMed ID: 4999589

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

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

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

  • 4. Phenotypic variation in Meckel syndrome.
    Seller MJ.
    Clin Genet; 1981 Jul; 20(1):74-7. PubMed ID: 7296953
    [Abstract] [Full Text] [Related]

  • 5. Meckel-Gruber syndrome.
    Ramachandran U, Malla T, Joshi KS.
    Kathmandu Univ Med J (KUMJ); 2006 Jul; 4(3):334-6. PubMed ID: 18603929
    [Abstract] [Full Text] [Related]

  • 6. [Meckel syndrome in 2 brothers. Clinical, anatomopathologic and genetic aspects].
    Restrepo CM, García-Cruz D, Sánchez G, Cantú JM.
    Bol Med Hosp Infant Mex; 1988 Sep; 45(9):600-4. PubMed ID: 3190852
    [No Abstract] [Full Text] [Related]

  • 7. Dandy-Walker malformation in the Meckel syndrome.
    Herriot R, Hallam LA, Gray ES.
    Am J Med Genet; 1991 May 01; 39(2):207-10. PubMed ID: 2063927
    [Abstract] [Full Text] [Related]

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

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

  • 10. Meckel Gruber syndrome--a single gene cause of recurrent neural tube defects.
    de Silva D, Suriyawansa D, Mangalika M, Samarasinghe D.
    Ceylon Med J; 2001 Mar 01; 46(1):30. PubMed ID: 11570001
    [Abstract] [Full Text] [Related]

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

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

  • 13. Phenotypic variability in Meckel-Gruber syndrome.
    Farag TI, Usha R, Uma R, Mady SA, al-Nagdy K, el-Badramany MH.
    Clin Genet; 1990 Sep 01; 38(3):176-9. PubMed ID: 2225527
    [Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of a case of ectrodactyly in 2D and 3D ultrasound.
    Kang A, Visca E, Bruder E, Holzgreve W, Struben H, Tercanli S.
    Ultraschall Med; 2009 Apr 01; 30(2):121-3. PubMed ID: 19421951
    [No Abstract] [Full Text] [Related]

  • 15. Meckel Gruber syndrome: occurrence in non-consanguineous marriages.
    de Silva MV, Senanayake H, Siriwardana KD.
    Ceylon Med J; 2004 Mar 01; 49(1):30-1. PubMed ID: 15255329
    [Abstract] [Full Text] [Related]

  • 16. An autosomal recessive syndrome of cleft palate, cardiac defect, genital anomalies, and ectrodactyly (CCGE).
    Giannotti A, Digilio MC, Mingarelli R, Dallapiccola B.
    J Med Genet; 1995 Jan 01; 32(1):72-4. PubMed ID: 7897634
    [Abstract] [Full Text] [Related]

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

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

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

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

    Page: [Next] [New Search]
    of 12.