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Pubmed for Handhelds

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Journal Abstract Search

159 related items for PubMed ID: 6646916

  • 21. [Classification--or present conceptions of associated malformations of the head and the extremities].
    Kissel P.
    Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg; 1969; 44(3-4):suppl 14-27. PubMed ID: 4255041
    [No Abstract] [Full Text] [Related]

  • 22. Ectopia cordis and chromosome errors.
    King CR.
    Pediatrics; 1980 Aug; 66(2):328. PubMed ID: 7402824
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  • 25. Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?
    Shashi V, Golden WL, von Kap-Herr C, Wilson WG.
    Am J Med Genet; 1996 Mar 01; 62(1):38-41. PubMed ID: 8779322
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  • 31. Double trisomy (48,XXX, +18).
    Tsukahara M, Fukuda M, Furukawa S, Kondoh O.
    Am J Med Genet; 1994 Aug 15; 52(2):244. PubMed ID: 7802021
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  • 32. Duplication (17p) in a child with an isodicentric (17p) chromosome.
    Mascarello JT, Jones MC, Hoyme HE, Freebury MM.
    Am J Med Genet; 1983 Jan 15; 14(1):67-72. PubMed ID: 6681937
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  • 37. Schmid-Fraccaro syndrome ("cat's eye" syndrome).
    Petersen RA.
    Arch Ophthalmol; 1973 Oct 15; 90(4):287-91. PubMed ID: 4746642
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  • 38. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
    Tschernigg M, Petek E, Leonhardtsberger A, Wagner K, Kroisel PM.
    Genet Couns; 2002 Oct 15; 13(3):303-7. PubMed ID: 12416638
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  • 40. [Familial Russell-syndrome (author's transl)].
    Schwingshackl A, Ganner E, Hammerer I.
    Padiatr Padol; 1974 Oct 15; 9(2):130-7. PubMed ID: 4823694
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