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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

527 related items for PubMed ID: 2986457

  • 21.
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  • 22. Dominantly inherited syndrome of microcephaly and cleft palate.
    Halal F.
    Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112
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  • 23.
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  • 24. Autosomal recessive acro-fronto-facio-nasal dysostosis associated with genitourinary anomalies.
    Richieri-Costa A, Montagnoli L, Kamiya TY.
    Am J Med Genet; 1989 May; 33(1):121-4. PubMed ID: 2750779
    [Abstract] [Full Text] [Related]

  • 25. Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism.
    Chudley AE, Rozdilsky B, Houston CS, Becker LE, Knoll JH.
    Am J Med Genet; 1985 Jan; 20(1):145-58. PubMed ID: 3970066
    [Abstract] [Full Text] [Related]

  • 26. Fryns syndrome: a new variable multiple congenital anomaly (MCA) syndrome.
    Lubinsky M, Severn C, Rapoport JM.
    Am J Med Genet; 1983 Mar; 14(3):461-6. PubMed ID: 6859098
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  • 27.
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  • 28. Frontofacionasal dysplasia: evidence for autosomal recessive inheritance.
    Gollop TR, Kiota MM, Martins RM, Lucchesi EA, Alvarenga Filho E.
    Am J Med Genet; 1984 Oct; 19(2):301-5. PubMed ID: 6439039
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  • 29.
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  • 30. Cranio-oculo-fronto-nasal malformation: a new MCA condition?
    Lopes VL, Campos NL, Maciel-Guerra AT.
    Clin Dysmorphol; 1997 Jan; 6(1):25-9. PubMed ID: 9018414
    [Abstract] [Full Text] [Related]

  • 31. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.
    Hennekam RC, Geerdink RA, Hamel BC, Hennekam FA, Kraus P, Rammeloo JA, Tillemans AA.
    Am J Med Genet; 1989 Dec; 34(4):593-600. PubMed ID: 2624276
    [Abstract] [Full Text] [Related]

  • 32.
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  • 33. Mesomelic limb shortness: a previously unreported autosomal recessive type.
    Reardon W, Hall CM, Slaney S, Huson SM, Connell J, al-Hilaly N, Fixsen J, Baraitser M, Winter RM.
    Am J Med Genet; 1993 Oct 01; 47(5):788-92. PubMed ID: 8267013
    [Abstract] [Full Text] [Related]

  • 34.
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  • 36. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.
    Blanchet P, Lefort G, Eglin MC, Rieu D, Sarda P.
    Genet Couns; 1993 Oct 01; 4(4):289-94. PubMed ID: 8110417
    [Abstract] [Full Text] [Related]

  • 37. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome.
    Richieri-Costa A, Pereira SC.
    Am J Med Genet; 1992 Mar 01; 42(5):681-7. PubMed ID: 1632438
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  • 38.
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  • 40. The neurofaciodigitorenal (NFDR) syndrome.
    Freire-Maia N, Pinheiro M, Opitz JM.
    Am J Med Genet; 1982 Mar 01; 11(3):329-36. PubMed ID: 7081297
    [Abstract] [Full Text] [Related]

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