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Journal Abstract Search

225 related items for PubMed ID: 8291524

  • 1. Familial Brachmann-de Lange syndrome: further evidence for autosomal dominant inheritance and review of the literature.
    Feingold M, Lin AE.
    Am J Med Genet; 1993 Nov 15; 47(7):1064-7. PubMed ID: 8291524
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  • 2. Brachmann-de Lange syndrome: evidence for autosomal dominant inheritance.
    Robinson LK, Wolfsberg E, Jones KL.
    Am J Med Genet; 1985 Sep 15; 22(1):109-15. PubMed ID: 4050846
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  • 3. Male-to-male transmission of mild Brachmann-de Lange syndrome.
    Chodirker BN, Chudley AE.
    Am J Med Genet; 1994 Sep 01; 52(3):331-3. PubMed ID: 7528973
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  • 4. Brachmann-de Lange syndrome: diagnostic difficulties posed by the mild phenotype.
    Saul RA, Rogers RC, Phelan MC, Stevenson RE.
    Am J Med Genet; 1993 Nov 15; 47(7):999-1002. PubMed ID: 8291544
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  • 5. Autosomal dominant inheritance of Brachmann-de Lange syndrome.
    Kozma C.
    Am J Med Genet; 1996 Dec 30; 66(4):445-8. PubMed ID: 8989465
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  • 10. Syndrome of microcephaly, Brachmann-de Lange-like facial changes, severe metatarsus adductus, and developmental delay: mild Brachmann-de Lange syndrome?
    Halal F, Silver K.
    Am J Med Genet; 1992 Feb 01; 42(3):381-6. PubMed ID: 1536185
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  • 12. Exclusively maternal transmission of autosomal dominant Brachmann-de Lange syndrome.
    de Die-Smulders C, Schrander-Stumpel C, Fryns JP, Theunissen P.
    Am J Med Genet; 1994 Sep 01; 52(3):363. PubMed ID: 7810572
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  • 15. Familial occurrence of Brachmann-de Lange syndrome.
    Bankier A, Haan E, Birrell R.
    Am J Med Genet; 1986 Sep 01; 25(1):163-5. PubMed ID: 3799716
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  • 16. [Brachmann-de Lange syndrome in 16 of our patients].
    Pankau R, Johannson W, Meinecke P.
    Monatsschr Kinderheilkd; 1990 Feb 01; 138(2):72-6. PubMed ID: 2320015
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  • 17. Mild Brachmann-de Lange syndrome. Delineation of the clinical phenotype, and characteristic behaviors in a six-year-old boy.
    Bay C, Mauk J, Radcliffe J, Kaplan P.
    Am J Med Genet; 1993 Nov 15; 47(7):965-8. PubMed ID: 7507294
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  • 18. On the variable expression of the Brachmann-de Lange syndrome.
    de Die-Smulders C, Theunissen P, Schrander-Stumpel C, Frijns JP.
    Clin Genet; 1992 Jan 15; 41(1):42-5. PubMed ID: 1633646
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  • 19. Autosomal dominant inheritance of the Kabuki make-up (Niikawa-Kuroki) syndrome.
    Halal F, Gledhill R, Dudkiewicz A.
    Am J Med Genet; 1989 Jul 15; 33(3):376-81. PubMed ID: 2801772
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  • 20. Pitt-Rogers-Danks syndrome: further delineation.
    Lizcano-Gil LA, García-Cruz D, García-Cruz O, Sánchez-Corona J.
    Am J Med Genet; 1995 Feb 13; 55(4):420-2. PubMed ID: 7762580
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