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PUBMED FOR HANDHELDS

Journal Abstract Search


298 related items for PubMed ID: 10319196

  • 21. Multiple pterygium syndrome.
    Chen H, Chang CH, Misra RP, Peters HA, Grijalva NS, Opitz JM.
    Am J Med Genet; 1980; 7(2):91-102. PubMed ID: 7468651
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  • 22. A new autosomal recessive disorder resembling Weaver syndrome.
    Teebi AS, Sundareshan TS, Hammouri MY, al-Awadi SA, al-Saleh QA.
    Am J Med Genet; 1989 Aug; 33(4):479-82. PubMed ID: 2596508
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  • 25. Cerebro-reno-digital syndrome in two sibs.
    Piantanida M, Tiberti A, Plebani A, Martelli P, Danesino C.
    Am J Med Genet; 1993 Sep 01; 47(3):420-2. PubMed ID: 8135292
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  • 27. Fuhrmann syndrome of right-angle bowed femora, absence of fibulae and digital anomalies: two further cases.
    Lipson AH, Kozlowski K, Barylak A, Marsden W.
    Am J Med Genet; 1991 Nov 01; 41(2):176-9. PubMed ID: 1785629
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  • 28. [Weill Marchesani syndrome. Report of a case].
    el Kettani A, Hamdani M, Rais L, el Belhadji M, Rachid R, Laouissi N, Zaghloul K, Amraoui A.
    J Fr Ophtalmol; 2001 Nov 01; 24(9):944-8. PubMed ID: 11912838
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  • 29. Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritance.
    Passos-Bueno MR, Marie SK, Monteiro M, Neustein I, Whittle MR, Vainzof M, Zatz M.
    Am J Med Genet; 1994 Aug 15; 52(2):170-3. PubMed ID: 7802003
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  • 36. Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly.
    Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1992 Feb 01; 42(3):340-2. PubMed ID: 1536175
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