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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

87 related items for PubMed ID: 2921511

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  • 2. Linkage of the hypodactyly and incisorless genes in the Norway rat.
    Moutier R.
    J Hered; 1980; 71(2):129-30. PubMed ID: 7391535
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  • 4. Wavy: a new recessive rexoid mutant in the Norway rat.
    Greaves JH.
    J Hered; 1981; 72(4):291-2. PubMed ID: 7288144
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  • 12. Fuzzy, a hypotrichotic mutant in linkage group I of the Norway rat.
    Palm J, Ferguson FG.
    J Hered; 1976; 67(5):284-8. PubMed ID: 1010929
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  • 13. Dense cataract and microphthalmia--new spontaneous mutation in BALB/c mice.
    Kohale K, Ingle A, Kelkar A, Parab P.
    Comp Med; 2004 Jun; 54(3):275-9. PubMed ID: 15253273
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  • 14. Age-resolving osteopetrosis: a rat model implicating microphthalmia and the related transcription factor TFE3.
    Weilbaecher KN, Hershey CL, Takemoto CM, Horstmann MA, Hemesath TJ, Tashjian AH, Fisher DE.
    J Exp Med; 1998 Mar 02; 187(5):775-85. PubMed ID: 9480987
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  • 17. Autosomal recessive colobomatous microphthalmia.
    Zlotogora J, Legum C, Raz J, Merin S, BenEzra D.
    Am J Med Genet; 1994 Feb 01; 49(3):261-2. PubMed ID: 8209881
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  • 19. CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindreds.
    Bar-Yosef U, Abuelaish I, Harel T, Hendler N, Ofir R, Birk OS.
    Hum Genet; 2004 Sep 01; 115(4):302-9. PubMed ID: 15257456
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  • 20. Osteopetrosis, a new recessive skeletal mutation on chromosome 12 of the mouse.
    Marks SC, Lane PW.
    J Hered; 1976 Sep 01; 67(1):11-18. PubMed ID: 1262696
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