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

171 related items for PubMed ID: 7726232

  • 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. Arthrogryposis, renal dysfunction and cholestasis syndrome.
    Abdullah MA, Al-Hasnan Z, Okamoto E, Abomelha AM.
    Saudi Med J; 2000 Mar; 21(3):297-9. PubMed ID: 11533803
    [Abstract] [Full Text] [Related]

  • 5. Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system.
    Illum N, Reske-Nielsen E, Skovby F, Askjaer SA, Bernsen A.
    Neuropediatrics; 1988 Nov; 19(4):186-92. PubMed ID: 3205375
    [Abstract] [Full Text] [Related]

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

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

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

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

  • 10. Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract.
    Cohen D, Bar-Yosef U, Levy J, Gradstein L, Belfair N, Ofir R, Joshua S, Lifshitz T, Carmi R, Birk OS.
    Invest Ophthalmol Vis Sci; 2007 May; 48(5):2208-13. PubMed ID: 17460281
    [Abstract] [Full Text] [Related]

  • 11. Ovine heritable arthrogryposis multiplex congenita with probable lethal autosomal recessive mutation.
    Tejedor MT, Ferrer LM, Monteagudo LV, Ramos JJ, Lacasta D, Climent S.
    J Comp Pathol; 2010 Jul; 143(1):14-9. PubMed ID: 20153865
    [Abstract] [Full Text] [Related]

  • 12. The distal arthrogryposes: delineation of new entities--review and nosologic discussion.
    Hall JG, Reed SD, Greene G.
    Am J Med Genet; 1982 Feb; 11(2):185-239. PubMed ID: 7039311
    [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. High incidence of autosomal recessive nonsyndromal congenital retinal nonattachment (NCRNA) in an Iranian founding population.
    Ghiasvand NM, Shirzad E, Naghavi M, Vaez Mahdavi MR.
    Am J Med Genet; 1998 Jul 07; 78(3):226-32. PubMed ID: 9677055
    [Abstract] [Full Text] [Related]

  • 17. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E, Goecke T, Meinecke P.
    Am J Med Genet; 1996 May 03; 63(1):185-9. PubMed ID: 8723107
    [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 9.