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PUBMED FOR HANDHELDS

Journal Abstract Search


159 related items for PubMed ID: 8213905

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  • 3. The Larsen syndrome, autosomal dominant form.
    Sugarman GI.
    Birth Defects Orig Artic Ser; 1975; 11(2):121-9. PubMed ID: 1227522
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  • 5. The Larsen syndrome occurring in four generations of one family.
    Stanley D, Seymour N.
    Int Orthop; 1985; 8(4):267-72. PubMed ID: 4018961
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  • 9. Severe cardiac anomalies in sibs with Larsen syndrome.
    Strisciuglio P, Sebastio G, Andria G, Maione S, Raia V.
    J Med Genet; 1983 Dec; 20(6):422-4. PubMed ID: 6655668
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  • 14. Congenital heart defects, hamartomas of the tongue and polysyndactyly in a sister and brother.
    Orstavik KH, Lindemann R, Solberg LA, Foerster A, Sørland SJ.
    Clin Genet; 1992 Jul; 42(1):19-21. PubMed ID: 1516223
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  • 15. Familial joint instability syndrome.
    Horton WA, Collins DL, DeSmet AA, Kennedy JA, Schimke RN.
    Am J Med Genet; 1980 Jul; 6(3):221-8. PubMed ID: 7424974
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  • 16. [Larsen's syndrome. Clinical findings and inheritance (author's transl)].
    Renault F, Arthuis M, Rethoré MO, Lafourcade J.
    Arch Fr Pediatr; 1982 Jan; 39(1):35-8. PubMed ID: 7065820
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  • 17. Acro-cardio-facial syndrome: a microdeletion syndrome?
    Toschi B, Valetto A, Bertini V, Congregati C, Cantinotti M, Assanta N, Simi P.
    Am J Med Genet A; 2012 Aug; 158A(8):1994-9. PubMed ID: 22740423
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  • 18. Larsen syndrome.
    Gupta N, Kabra M.
    Indian Pediatr; 2008 Sep; 45(9):783-4. PubMed ID: 18820390
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  • 19. Separating Larsen syndrome from the "arthrogryposis basket".
    Houston CS, Reed MH, Desautels JE.
    J Can Assoc Radiol; 1981 Dec; 32(4):206-14. PubMed ID: 7328098
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