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Journal Abstract Search

358 related items for PubMed ID: 491337

  • 1. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
    Pai GS, Thomas GH, Leonard CO, Ward JC, Valle DL, Pyeritz RE.
    Johns Hopkins Med J; 1979 Oct; 145(4):162-9. PubMed ID: 491337
    [No Abstract] [Full Text] [Related]

  • 2. Autosomal syndromes.
    Summitt RL.
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
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  • 3. Duplication (partial trisomy) of the distal long arm of chromosome 17: a new clinically recognizable chromosome disorder.
    Berberich MS, Carey JC, Lawce HJ, Hall BD.
    Birth Defects Orig Artic Ser; 1978 Jun; 14(6C):287-95. PubMed ID: 728583
    [No Abstract] [Full Text] [Related]

  • 4. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
    Taysi K, Dengler DR, Jones LA, Heersma JR.
    Ann Genet; 1981 Jun; 24(4):245-7. PubMed ID: 7036843
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  • 7. Deletion of 11q: report of two cases and a review.
    Larson SA, Yeatman GW, Riccardi VM.
    Birth Defects Orig Artic Ser; 1976 Jun; 12(5):125-30. PubMed ID: 953212
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  • 8. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
    Wilson MG, Towner JW, Forsman I, Siris E.
    Am J Med Genet; 1979 Jun; 3(2):155-74. PubMed ID: 474629
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  • 9. Cri du chat-syndrome in combination with partial trisomy 9 p.
    Sigmund J, Frisch H, Heinz-Erian P, Rhomberg K, Wegner RD.
    Padiatr Padol; 1986 Jun; 21(1):61-7. PubMed ID: 3960564
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  • 11. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
    Fryns JP, Kleczkowska A, Kenis H, Decock P, Van den Berghe H.
    Ann Genet; 1989 Jun; 32(3):174-6. PubMed ID: 2573314
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  • 14. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A, Delicado A, Izquierdo M, Oliver A, López Pajares I, Gracia R, Peralta A.
    An Esp Pediatr; 1981 May; 14(5):344-51. PubMed ID: 7294523
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  • 15. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA, Mikel'saar AV, Mikel'saar RV.
    Sov Genet; 1974 Jun 01; 8(5):651-7. PubMed ID: 4413436
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