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PUBMED FOR HANDHELDS

Journal Abstract Search


171 related items for PubMed ID: 3833759

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  • 2. [Syndrome of congenital defects of the heart, eye and osseous system].
    Szczeklik E, Strózyna-Kotulska W, Kustrzycki A, Olichwier B, Bross T.
    Przegl Lek; 1976; 33(4):479-81. PubMed ID: 818682
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  • 4. [Case of "upper limb-cardiovascular syndrome" (Holt-Oram syndrome)].
    Polimeno M, Fadda C, Abate M, Morieri M, Del Vecchio E.
    Minerva Pediatr; 1982 Jun 15; 34(11):511-6. PubMed ID: 7132932
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  • 6. Limb abnormalities and mental retardation.
    Smith GF, Schindeler J, Elbualy S, Shear C.
    J Ment Defic Res; 1970 Dec 15; 14(4):319-41. PubMed ID: 5517969
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  • 10. A case of Holt Oram syndrome.
    Abhayambika K, Girija G, Joseph J.
    Indian Heart J; 1991 Dec 15; 43(1):59-60. PubMed ID: 1894307
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  • 13. Reduction malformations and chromosome anomalies.
    Bofinger MK, Dignan PS, Schmidt RE, Warkany J.
    Am J Dis Child; 1973 Jan 15; 125(1):135-43. PubMed ID: 4346056
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  • 14. Syndrome of a craniofacial dysostosis, limb malformation, and omphalocele.
    Gardner RJ, Morrison PS, Faigan LA, Kennedy JC, Fitzgerald PH.
    Am J Med Genet; 1990 Jun 15; 36(2):133-6. PubMed ID: 2368799
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  • 15. Congenital triangular alopecia in association with congenital heart diseases, bone and teeth abnormalities, multiple lentigines and café-au-lait patches.
    Park SW, Choi YD, Wang HY.
    Int J Dermatol; 2004 May 15; 43(5):366-7. PubMed ID: 15117369
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  • 16. Six generations of a family with multiple limb deficiencies.
    Helal A, Perry T, Ogden JA, Greene TL.
    J Pediatr Orthop; 1993 May 15; 13(2):210-3. PubMed ID: 8459013
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  • 20. Q--congenital hemidysplasia with ichthyosis.
    Tang TT, McCreadie SR.
    Birth Defects Orig Artic Ser; 1974 May 15; 10(5):257-61. PubMed ID: 4620143
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