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

139 related items for PubMed ID: 7211958

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. [Mental retardation and X chromosome fragility].
    Rodríguez de la Rúa V, Alvárez García F, Hernando I, Benavides A, Coto GD, de Juan J, Fernández Toral J.
    An Esp Pediatr; 1986 Nov; 25(5):329-34. PubMed ID: 3813225
    [Abstract] [Full Text] [Related]

  • 26. Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of X-linked mental retardation.
    Howard-Peebles PN.
    Am J Med Genet; 1980 Nov; 7(4):497-501. PubMed ID: 6938133
    [Abstract] [Full Text] [Related]

  • 27. Linkage analysis in three families with nonspecific X-linked mental retardation.
    Claes S, Gu XX, Legius E, Lorenzetti E, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P.
    Am J Med Genet; 1996 Jul 12; 64(1):137-46. PubMed ID: 8826464
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. Familial X-linked mental retardation syndrome associated with minor congenital anomalies, macro-orchidism, and fragile X-chromosome.
    Pueschel SM, Hays RM, Mendoza T.
    Am J Ment Defic; 1983 Jan 12; 87(4):372-6. PubMed ID: 6829615
    [Abstract] [Full Text] [Related]

  • 30. New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3.
    Wittwer B, Kircheisen R, Leutelt J, Orth U, Gal A.
    Am J Med Genet; 1996 Jul 12; 64(1):42-9. PubMed ID: 8826447
    [Abstract] [Full Text] [Related]

  • 31. Pentasomy X: report of patient and studies of X-inactivation.
    Funderburk SJ, Valente M, Klisak I.
    Am J Med Genet; 1981 Jul 12; 8(1):27-33. PubMed ID: 7246603
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation.
    Proops R, Webb T.
    J Med Genet; 1981 Oct 12; 18(5):366-73. PubMed ID: 7328617
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28.
    Hamel BC, Kremer H, Wesby-van Swaay E, van den Helm B, Smits AP, Oostra BA, Ropers HH, Mariman EC.
    Am J Med Genet; 1996 Jul 12; 64(1):131-3. PubMed ID: 8826463
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).
    Claes S, Vogels A, Holvoet M, Devriendt K, Raeymaekers P, Cassiman JJ, Fryns JP.
    Am J Med Genet; 1997 Dec 31; 73(4):474-9. PubMed ID: 9415477
    [Abstract] [Full Text] [Related]

  • 39. Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38).
    Schutz CK, Ives EJ, Chalifoux M, MacLaren L, Farrell S, Robinson PD, White BN, Holden JJ.
    Am J Med Genet; 1996 Jul 12; 64(1):89-96. PubMed ID: 8826457
    [Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 7.