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Journal Abstract Search

86 related items for PubMed ID: 1466568

  • 21.
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  • 23. 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; 205(3):162-6. PubMed ID: 8350589
    [Abstract] [Full Text] [Related]

  • 24. Terminal deletion 6p23: a case report.
    Kormann-Bortolotto MH, Farah LM, Soares D, Corbani M, Müller R, Adell AC.
    Am J Med Genet; 1990 Dec; 37(4):475-7. PubMed ID: 2260591
    [Abstract] [Full Text] [Related]

  • 25. Further experience in the management of craniofacial dysmorphic states.
    Nagib MG, Wisiol ES, Shilling BB, Purcell TW, Tubman DE.
    Minn Med; 1985 Jul; 68(7):521-5. PubMed ID: 4021967
    [No Abstract] [Full Text] [Related]

  • 26. Freeman Sheldon syndrome.
    Goyel NA, Patel ZM, Wagle PB, Mulye VR.
    Indian Pediatr; 1986 Feb; 23(2):146-8. PubMed ID: 3710569
    [No Abstract] [Full Text] [Related]

  • 27. Monosomy 8p: an easily overlooked syndrome.
    Bröcker-Vriends AH, Mooij PD, van Bel F, Beverstock GC, van de Kamp JJ.
    J Med Genet; 1986 Apr; 23(2):153-4. PubMed ID: 3712390
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  • 29. Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32----qter.
    Al-Awadi SA, Teebi AS, Sundareshan TS.
    Ann Genet; 1985 Apr; 28(3):181-4. PubMed ID: 3879154
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  • 33. 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
    [Abstract] [Full Text] [Related]

  • 34. Association of 13q deletion and Hirschsprung's disease.
    Kiss P, Osztovics M.
    J Med Genet; 1989 Dec; 26(12):793-4. PubMed ID: 2614805
    [No Abstract] [Full Text] [Related]

  • 35. Deletion of chromosome 13 in Moebius syndrome.
    Slee JJ, Smart RD, Viljoen DL.
    J Med Genet; 1991 Jun; 28(6):413-4. PubMed ID: 1870098
    [Abstract] [Full Text] [Related]

  • 36. Infant cephalometrics as a research tool for the comprehensive study of newborns with facial anomalies.
    Berkowitz S.
    J Fla Med Assoc; 1968 Feb; 55(2):100-1. PubMed ID: 5746933
    [No Abstract] [Full Text] [Related]

  • 37. [Craniofacial dysmorphism in pediatric AIDS. Presentation of a case].
    González Núñez I, Díaz Jidy M, Capó de Paz V, Rodríguez Barreras ME.
    Rev Cubana Med Trop; 1994 Feb; 46(1):60-4. PubMed ID: 9768237
    [Abstract] [Full Text] [Related]

  • 38. Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism.
    Fryns JP, Kleczkowska A, Van Den Berghe H.
    Genet Couns; 1990 Feb; 1(2):173-7. PubMed ID: 2081001
    [No Abstract] [Full Text] [Related]

  • 39. The 8p-syndrome.
    Ostergaard GZ, Tommerup N.
    Ann Genet; 1989 Feb; 32(2):87-91. PubMed ID: 2667457
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  • 40.
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