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

256 related items for PubMed ID: 566736

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

  • 5. Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals.
    Hauksdóttir H, Halldórsson S, Jensson O, Mikkelsen M, McDermott A.
    J Med Genet; 1972 Dec; 9(4):413-21. PubMed ID: 4646548
    [No Abstract] [Full Text] [Related]

  • 6. Studies of malformation syndromes in man. XXVII. The N syndrome, a "new" multiple congenital anomaly-mental retardation syndrome.
    Hess RO, Kaveggia EG, Opitz JM.
    Clin Genet; 1974 Dec; 6(4):237-46. PubMed ID: 4216437
    [No Abstract] [Full Text] [Related]

  • 7. Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.
    Weber FM, Sparkes RS, Muller H.
    Cytogenetics; 1971 Dec; 10(6):404-12. PubMed ID: 5146417
    [No Abstract] [Full Text] [Related]

  • 8. Chromosome studies in patients with congenital malformations and mental retardation.
    Erdtmann B, Salzano FM, Mattevi MS.
    Humangenetik; 1975 Dec; 26(4):297-306. PubMed ID: 1150230
    [Abstract] [Full Text] [Related]

  • 9. X-linked mental retardation with macro-orchidism and marker X chromosomes.
    Howard-Peebles PN, Stoddard GR.
    Hum Genet; 1979 Sep; 50(3):247-51. PubMed ID: 489008
    [Abstract] [Full Text] [Related]

  • 10. A new form of X-linked mental retardation with growth retardation, deafness, and microgenitalism.
    Juberg RC, Marsidi I.
    Am J Hum Genet; 1980 Sep; 32(5):714-22. PubMed ID: 6107045
    [Abstract] [Full Text] [Related]

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

  • 12. Retinal pigment mosaicism in Pallister-Killian syndrome (mosaic tetrasomy 12p).
    Graham W, Brown SM, Shah F, Tonk VS, Kukolich MK.
    Arch Ophthalmol; 1999 Dec; 117(12):1648-9. PubMed ID: 10604674
    [No Abstract] [Full Text] [Related]

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

  • 14. 49,XXXXX syndrome.
    Fragoso R, Hernandez A, Plascencia ML, Nazara Z, Martinez y Martinez R, Cantu JM.
    Ann Genet; 1982 Dec; 25(3):145-8. PubMed ID: 6982661
    [Abstract] [Full Text] [Related]

  • 15. Retinitis pigmentosa, mental retardation, marked short stature, and brachydactyly in two sibs.
    Lorda-Sanchez I, Trujillo MJ, Gimenez A, Garcia-Sandoval B, Franco A, Sanz R, Rodriguez de Alba M, Ramos C, Ayuso C.
    Ophthalmic Genet; 1999 Jun; 20(2):127-31. PubMed ID: 10420199
    [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. Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother.
    Tabor A, Andersen O, Lundsteen C, Niebuhr E, Sardemann H.
    Hum Genet; 1983 Jun; 64(2):196-9. PubMed ID: 6885061
    [Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 13.