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PUBMED FOR HANDHELDS

Journal Abstract Search


191 related items for PubMed ID: 6808331

  • 21. Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomalies.
    Sensi A, Bettoli V, Zampino MR, Gandini E, Calzolari E.
    Am J Med Genet; 1994 Apr 01; 50(2):201-3. PubMed ID: 8010352
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  • 22. An apparently new acrocraniofacial syndrome with cranial nerve and visceral anomalies.
    Hameed R, Bissenden JG, Webb WR, Cole TR.
    Clin Dysmorphol; 1999 Jul 01; 8(3):199-202. PubMed ID: 10457854
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  • 24. Costello syndrome and facio-cutaneous-skeletal syndrome.
    Philip N, Mancini J.
    Am J Med Genet; 1993 Aug 15; 47(2):174-5. PubMed ID: 8213902
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  • 27. Abnormal hair, craniofacial dysmorphism, and severe mental retardation - a new syndrome?
    Killian W, Zonana J, Schroer RJ.
    J Clin Dysmorphol; 1983 Aug 15; 1(3):6-13. PubMed ID: 6584560
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  • 28. [The Cohen syndrome. Presentation of the 1st Italian case].
    De Toni T, Naselli A, Cafiero V, Bagnara V, Cavaliere GG, Duillo MT.
    Minerva Pediatr; 1982 Mar 31; 34(6):261-6. PubMed ID: 6808330
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  • 29. [Deletion of the short arm of chromosome 4].
    Hurgoiu V, Lazăr Garoiu F, Giurgiuman M, Rusu S.
    Rev Pediatr Obstet Ginecol Pediatr; 1980 Mar 31; 29(3):243-8. PubMed ID: 6110234
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  • 33. Syndrome of arachnodactyly, disturbance of cranial ossification, protruding eyes, feeding difficulties, and mental retardation.
    Kosztolányi G, Weisenbach J, Méhes K.
    Am J Med Genet; 1995 Sep 11; 58(3):213-6. PubMed ID: 8533819
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  • 34. [Cranio-carpo-tarsal dysplasia syndrome (Freeman-Sheldon syndrome, whistling face syndrome)].
    Träger D.
    Z Orthop Ihre Grenzgeb; 1987 Sep 11; 125(1):106-7. PubMed ID: 3577337
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  • 35. [Freeman-Sheldon syndrome: clinical manifestations and anesthetic and surgical management].
    Alonso Calderón JL, Ali Taoube K.
    An Esp Pediatr; 2002 Feb 11; 56(2):175-9. PubMed ID: 11827658
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  • 40. Radial ray defects, triangular face, telecanthus, sparse hair, dwarfism, and mental retardation.
    Imaizumi K, Kuroki Y.
    Am J Med Genet; 1991 Nov 01; 41(2):162-3. PubMed ID: 1785626
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