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Journal Abstract Search

349 related items for PubMed ID: 8031534

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  • 4. Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7p due to a de novo tandem duplication 7 (p15.1-->p21.3).
    Kleczkowska A, Decock P, van den Berghe H, Fryns JP.
    Genet Couns; 1994; 5(4):393-7. PubMed ID: 7888144
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  • 7. [Clinical picture of partial monosomy of chromosome 11 q].
    Dörr U.
    Monatsschr Kinderheilkd; 1986 Nov; 134(11):808-11. PubMed ID: 3807920
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  • 8. 16q21 is critical for 16q deletion syndrome.
    Naritomi K, Shiroma N, Izumikawa Y, Sameshima K, Ohdo S, Hirayama K.
    Clin Genet; 1988 May; 33(5):372-5. PubMed ID: 3378367
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  • 9. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
    van Balkom ID, Hagendoorn J, De Pater JM, Hennekam RC.
    Genet Couns; 1992 May; 3(2):83-9. PubMed ID: 1642815
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  • 10. Aminopterin Syndrome Sine Aminopterin (ASSA) syndrome in two siblings: further delineation of the syndrome and review of the literature.
    Krajewska-Walasek M.
    Genet Couns; 1994 May; 5(4):345-55. PubMed ID: 7888136
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  • 12. Interstitial deletion of (17)(p11.2p11.2) in nine patients.
    Smith AC, McGavran L, Robinson J, Waldstein G, Macfarlane J, Zonona J, Reiss J, Lahr M, Allen L, Magenis E.
    Am J Med Genet; 1986 Jul; 24(3):393-414. PubMed ID: 2425619
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  • 14. Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literature.
    Fischer H, Oswald HP, Duba HC, Doczy L, Simma B, Utermann G, Haas OA.
    Klin Padiatr; 1993 Jul; 205(3):162-6. PubMed ID: 8350589
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  • 19. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.
    Pfeiffer RA, Legat G, Trautmann U.
    Ann Genet; 1992 Jul; 35(1):41-6. PubMed ID: 1610119
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