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PUBMED FOR HANDHELDS

Journal Abstract Search

173 related items for PubMed ID: 8775424

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  • 3. New autosomal dominant syndrome resembling craniofrontonasal dysplasia.
    Teebi AS.
    Am J Med Genet; 1987 Nov; 28(3):581-91. PubMed ID: 3425628
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  • 5. "C" trigonocephaly syndrome with diaphragmnatic hernia.
    Addor MC, Stefanutti D, Farron F, Meinecke P, Lacombe D, Sarlangue J, Prescia G, Schorderet DF.
    Genet Couns; 1995 Nov; 6(2):113-20. PubMed ID: 7546453
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  • 8. [Coffin-Lowry syndrome and hyperprolinemia].
    Lacombe D, Parrot-Roulaud F, Castell JF, Serville F, Hehunstre JP, Battin J.
    Arch Fr Pediatr; 1993 Nov; 50(6):489-92. PubMed ID: 8135609
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  • 10. 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
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  • 11. New syndrome: mother and son with hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies.
    Seaver LH, Cassidy SB.
    Am J Med Genet; 1991 Dec 15; 41(4):405-9. PubMed ID: 1776627
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  • 13. Clinical and genetic aspects of craniofrontonasal syndrome: towards resolving a genetic paradox.
    Wieacker P, Wieland I.
    Mol Genet Metab; 2005 Dec 15; 86(1-2):110-6. PubMed ID: 16143553
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  • 14. Craniofrontonasal dysplasia.
    Hurst J, Baraitser M.
    J Med Genet; 1988 Feb 15; 25(2):133-4. PubMed ID: 3346887
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  • 16. Zimmermann-Laband syndrome in a patient with severe mental retardation.
    Van Buggenhout GJ, Brunner HG, Trommelen JC, Hamel BC.
    Genet Couns; 1995 Feb 15; 6(4):321-7. PubMed ID: 8775419
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  • 18. Costello syndrome: the natural history of a true postnatal growth retardation syndrome.
    Umans S, Decock P, Fryns JP.
    Genet Couns; 1995 Feb 15; 6(2):121-5. PubMed ID: 7546454
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