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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

189 related items for PubMed ID: 3756012

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  • 5. Ptosis, down-slanting palpebral fissures, hypertelorism, seizures and mental retardation: a possible new MCA/MR syndrome.
    Mégarbané A, Le Merrer M, el Kallab K.
    Clin Dysmorphol; 1997 Jul; 6(3):239-44. PubMed ID: 9220194
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  • 9. Autosomal recessive Robinow syndrome.
    Teebi AS.
    Am J Med Genet; 1990 Jan; 35(1):64-8. PubMed ID: 2301471
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  • 11. Greig cephalopolysyndactyly: report of 13 affected individuals in three families.
    Baraitser M, Winter RM, Brett EM.
    Clin Genet; 1983 Oct; 24(4):257-65. PubMed ID: 6641002
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  • 12. Hypertelorism, proptosis, ptosis, polysyndactyly, hypospadias and normal height in 3 sibs: a new syndrome?
    Naguib KK.
    Am J Med Genet; 1988 Jan; 29(1):35-41. PubMed ID: 2830788
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  • 13. Delineation of a characteristic phenotype in distal trisomy 2q.
    Kyllerman M, Wahlström J, Westerberg B, Gustavson KH.
    Helv Paediatr Acta; 1984 Dec; 39(5-6):499-508. PubMed ID: 6543860
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  • 18. Multiple lentigines syndrome in a Nigerian family.
    Kubeyinje EP, Onunu AN, Obasohan AO.
    Trop Geogr Med; 1993 Dec; 45(3):135-7. PubMed ID: 8362457
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  • 20. Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13).
    Krüger G, Götz J, Kvist U, Dunker H, Erfurth F, Pelz L, Zech L.
    Am J Med Genet; 1989 Mar; 32(3):411-6. PubMed ID: 2729360
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