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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

128 related items for PubMed ID: 2240027

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  • 4. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
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  • 5. A child with sclerocornea, short limbs, short stature, and distinct facial appearance.
    Thompson EM, Winter RM.
    Am J Med Genet; 1988 Jul 01; 30(3):719-24. PubMed ID: 3055984
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  • 8. The Cohen syndrome in Israel.
    Sack J, Friedman E.
    Isr J Med Sci; 1986 Nov 01; 22(11):766-70. PubMed ID: 2432032
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  • 9. Further delineation of the Cohen syndrome; report on chorioretinal dystrophy, leukopenia and consanguinity.
    Norio R, Raitta C, Lindahl E.
    Clin Genet; 1984 Jan 01; 25(1):1-14. PubMed ID: 6705238
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  • 16. A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews.
    Auslender N, Sharon D, Abbasi AH, Garzozi HJ, Banin E, Ben-Yosef T.
    Invest Ophthalmol Vis Sci; 2007 Dec 01; 48(12):5431-8. PubMed ID: 18055789
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  • 17. Possible new type of oral-facial-digital syndrome with retinal abnormalities: OFDS type (VIII).
    Gurrieri F, Sammito V, Ricci B, Iossa M, Bellussi A, Neri G.
    Am J Med Genet; 1992 Apr 01; 42(6):789-92. PubMed ID: 1554016
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  • 20. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
    Chitayat D, Hall JG, Couch RM, Phang MS, Baldwin VJ.
    Am J Med Genet; 1990 Sep 01; 37(1):65-70. PubMed ID: 2240046
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