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Journal Abstract Search

161 related items for PubMed ID: 3692885

  • 1. Distal 11q deletion: a specific clinical entity.
    Fryns JP, Kleczkowska A, Smeets E, Van den Berghe H.
    Helv Paediatr Acta; 1987 Oct; 42(2-3):191-4. PubMed ID: 3692885
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  • 2. Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.
    Obregon MG, Mingarelli R, Digilio MC, Zelante L, Giannotti A, Sabatino G, Dallapiccola B.
    Ann Genet; 1992 Oct; 35(4):208-12. PubMed ID: 1296516
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  • 3. 11q- syndrome: three cases and a review of the literature.
    Leegte B, Kerstjens-Frederikse WS, Deelstra K, Begeer JH, van Essen AJ.
    Genet Couns; 1999 Oct; 10(3):305-13. PubMed ID: 10546104
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  • 6. Brief clinical report: deletion of the long arm of chromosome 11, [del(11)(q23)].
    Monteleone PL, Chen SC, Nouri-Moghaddam S, Blair JD, Tietjens M.
    Am J Med Genet; 1982 Nov; 13(3):299-304. PubMed ID: 6891182
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  • 7. Monosomy 11Q: report of new phenotypic manifestations.
    Puvabanditsin S, Garrow E, Zia-Ullah MO, Supavekin S, Lianthanasarn P, Denev KI.
    Genet Couns; 2001 Nov; 12(3):283-6. PubMed ID: 11693793
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  • 9. Deletion of the distal long arm of chromosome 1: a definable syndrome.
    Johnson VP, Heck LJ, Carter GA, Flom JO.
    Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
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  • 10. Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.
    Fryns JP, Yang-Aisheng, Kleczkowska A, Lemmens F, Vandecasseye W, van den Berghe H.
    Ann Genet; 1989 Dec; 32(1):59-61. PubMed ID: 2751251
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  • 11. [Deletion 11q23 --> qter (Jacobsen Syndrome) associated with duodenal atresia and annular pancreas].
    Fernández González N, Prieto Espuñes S, Ibáñez Fernández A, Fernández Colomer B, López Sastre J, Fernández Toral J.
    An Esp Pediatr; 2002 Sep; 57(3):249-52. PubMed ID: 12199949
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  • 12. Deletion of proximal 6q: a clinical report and review of the literature.
    Yamamoto Y, Okamoto N, Shiraishi H, Yanagisawa M, Kamoshita S.
    Am J Med Genet; 1986 Nov; 25(3):467-71. PubMed ID: 3789009
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  • 16. De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis.
    Fryns JP, Haspeslagh M, Agneessens A, van den Berghe H.
    Ann Genet; 1985 Nov; 28(1):45-8. PubMed ID: 3874588
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  • 17. Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37).
    Wang TH, Johnston K, Hsieh CL, Dennery PA.
    Am J Med Genet; 1994 Feb 15; 49(4):399-401. PubMed ID: 8160733
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  • 18. Jacobsen syndrome: chromosome deletion at 11q23.
    Clang DR, LaBaere RJ.
    J Am Osteopath Assoc; 1998 Oct 15; 98(10):551-4. PubMed ID: 9821738
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  • 19. Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24).
    Gadzicki D, Baumer A, Wey E, Happel CM, Rudolph C, Tönnies H, Neitzel H, Steinemann D, Welte K, Klein C, Schlegelberger B.
    Ann Hum Genet; 2006 Nov 15; 70(Pt 6):958-64. PubMed ID: 17044870
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