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Journal Abstract Search

582 related items for PubMed ID: 8469651

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  • 4. Antley-Bixler syndrome: case report and review of the literature.
    Poddevin F, Delobel B, Courreges P, Bayart M.
    Genet Couns; 1995; 6(3):241-6. PubMed ID: 8588853
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  • 7. [Fatal genetic-morphologic syndromes. The campomelic syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 May; 14(3):162-4. PubMed ID: 8516273
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  • 9. Further delineation of the Yunis-Varon syndrome.
    Hennekam RC, Vermeulen-Meiners C.
    J Med Genet; 1989 Jan; 26(1):55-8. PubMed ID: 2918527
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  • 12. Schinzel-Giedion syndrome. A patient with hypothyroidism and diabetes insipidus.
    Santos H, Cordeiro I, Medeira A, Mendonça E, Antunes NL, Rosa FC.
    Genet Couns; 1994 Jan; 5(2):187-9. PubMed ID: 7917131
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  • 13. [Meckel-Gruber syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Jan; 14(1):32-5. PubMed ID: 8451225
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  • 14. [A child with Zellweger's cerebrohepatorenal syndrome].
    Govaerts L, Corstiaensen J, Bakkeren J, Trujbels F, Monnens L.
    Tijdschr Kindergeneeskd; 1983 Apr; 51(2):65-7. PubMed ID: 6879587
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  • 15. [Transverse extremity defects in a case of Adams-Oliver syndrome].
    Fehlow P, Walther F.
    Padiatr Grenzgeb; 1990 Apr; 29(4):279-84. PubMed ID: 2216522
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  • 16. A practical application of fluorescent in situ hybridization to the Wolf-Hirschhorn syndrome.
    Fagan K, Colley P, Partington M.
    Pediatrics; 1994 May; 93(5):826-7. PubMed ID: 8165089
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  • 17. Ectrodactyly, ectodermal dysplasia and cleft lip syndrome.
    Yap HK, Lee BW, Tay JS, Wong HB.
    J Singapore Paediatr Soc; 1985 May; 27(3-4):215-7. PubMed ID: 3831606
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  • 19. Opitz C syndrome and pseudohypoaldosteronism.
    De Koster J, Legius E, de Zegher F, Devlieger H, Fryns JP, Eggermont E.
    Am J Med Genet; 1990 Dec; 37(4):457-9. PubMed ID: 2175542
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  • 20. [Delayed bone growth as a sonographic sign in the early detection of Smith-Lemli-Opitz syndrome].
    Degenhardt F, Mühlhaus K.
    Z Geburtshilfe Perinatol; 1988 Dec; 192(4):169-72. PubMed ID: 3055721
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