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Journal Abstract Search

380 related items for PubMed ID: 6829599

  • 21. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
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  • 22. Short rib syndrome Beemer-Langer type with polydactyly: a multiple congenital anomalies syndrome.
    Yang SS, Roth JA, Langer LO.
    Am J Med Genet; 1991 Jun 01; 39(3):243-6. PubMed ID: 1867272
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  • 26. [Multisynostotic osterodysgenesis and the problem of genetic counseling in newly-identified syndromes (author's transl)].
    Delozier CD, Engel E.
    J Genet Hum; 1981 Sep 01; 29(3):365-77. PubMed ID: 7334357
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  • 27. Severe case of Al Awadi/Raas-Rothschild syndrome or new, possibly autosomal recessive facio-skeleto-genital syndrome.
    Mollica F, Mazzone D, Cimino G, Opitz JM.
    Am J Med Genet; 1995 Mar 27; 56(2):168-72. PubMed ID: 7625440
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  • 29. The Neu-Laxova syndrome in female sibs: clinical and pathological features with prenatal diagnosis in the second sib.
    Tolmie JL, Mortimer G, Doyle D, McKenzie R, McLaurin J, Neilson JP.
    Am J Med Genet; 1987 May 27; 27(1):175-82. PubMed ID: 3300330
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  • 30. A further case of opsismodysplasia with hydrocephalus.
    Ramos FJ, González JP, Cortabarria C, Domenech E, Pérez-González J, Bueno M.
    Eur J Med Genet; 2006 May 27; 49(1):93-100. PubMed ID: 16473316
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  • 31. Fountain syndrome: further delineation of the clinical syndrome and follow-up data.
    Van Buggenhout GJ, Van Ravenswaaij-Arts CM, Renier WO, Van de Wiel MP, Trommelen JC, Pijkels E, Hamel BC, Fryns JP.
    Genet Couns; 1996 May 27; 7(3):177-86. PubMed ID: 8897038
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  • 32. Beemer-Langer syndrome with manifestations of an orofaciodigital syndrome.
    Lin AE, Doshi N, Flom L, Tenenholz B, Filkins KL.
    Am J Med Genet; 1991 Jun 01; 39(3):247-51. PubMed ID: 1867273
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  • 35. Acrocallosal syndrome in two African brothers born to consanguineous parents.
    Christianson AL, Venter PA, Du Toit JL, Shipalana N, Gericke GS.
    Am J Med Genet; 1994 Jun 01; 51(2):98-101. PubMed ID: 8092201
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  • 37. 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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  • 38. Roberts syndrome or "X-linked amelia"?
    Gershoni-Baruch R, Drugan A, Bronshtein M, Zimmer EZ.
    Am J Med Genet; 1990 Dec 01; 37(4):569-72. PubMed ID: 2260610
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  • 39. Trisomy 8 syndrome. The rib anomaly and some new features in two cases.
    Annerén G, Frodis E, Jorulf H.
    Helv Paediatr Acta; 1981 Nov 01; 36(5):465-72. PubMed ID: 7309535
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  • 40. Oto-palato-digital syndrome with features of type I and II in brothers.
    Horn D, Nitz I, Bollmann R.
    Genet Couns; 1995 Nov 01; 6(3):233-40. PubMed ID: 8588852
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