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Journal Abstract Search


208 related items for PubMed ID: 4050847

  • 1. Further delineation of the dup(3q) syndrome.
    Wilson GN, Dasouki M, Barr M.
    Am J Med Genet; 1985 Sep; 22(1):117-23. PubMed ID: 4050847
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  • 2. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P, Adkins WN, Caspar H, Dumars KW, Gebauer J, Gilbert EF, Grimm T, Habedank M, Hansmann I, Herrmann J, Kaveggia EG, Langenbeck U, Meisner LF, Najafzadeh TM, Opitz JM, Palmer CG, Peters HH, Scholz W, Tavares AS, Wiedeking C.
    Am J Med Genet; 1981 Sep; 10(2):159-77. PubMed ID: 7315873
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  • 3. [Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].
    Ayral D, Raudrant D, Charleux JP, Noel B.
    Pediatrie; 1984 Dec; 39(8):681-90. PubMed ID: 6598632
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  • 12. Duplication 3q(q21----qter) without limb anomalies.
    Ismail SR, Kousseff BG, Kotb SM, Kholeif SF.
    Am J Med Genet; 1991 Mar 15; 38(4):518-22. PubMed ID: 2063889
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  • 14. Duplication of distal 15q: report of five new cases from two different translocation kindreds.
    Lacro RV, Jones KL, Mascarello JT, Jones OW, Wilson N, Jones MC.
    Am J Med Genet; 1987 Mar 15; 26(3):719-28. PubMed ID: 3565485
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  • 19. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC.
    Pediatrics; 2008 Feb 15; 121(2):404-10. PubMed ID: 18245432
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