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Journal Abstract Search

378 related items for PubMed ID: 2817777

  • 1. The 18p- syndrome. Report of five cases.
    Zumel RM, Darnaude MT, Delicado A, Diaz de Bustamante A, de Torres ML, López-Pájares I.
    Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
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  • 2. 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; 24(4):245-7. PubMed ID: 7036843
    [No Abstract] [Full Text] [Related]

  • 3. 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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  • 4. [Wolf syndrome. Apropos of 2 cases].
    García González P, Pedraz García C, Merino Marcos L, Salazar Veloz J, Escudero Bueno G, Salazar Villalobos V.
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
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  • 8. IgA deficiency associated with growth hormone deficiency in a boy with short arm deletion of chromosome 18 (46,XY,18p-).
    Gül D, Sayli BS, Gök F, Gökçay E.
    Ann Genet; 1994 Feb; 37(2):82-5. PubMed ID: 7527197
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  • 9. 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 Feb; 32(3):174-6. PubMed ID: 2573314
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  • 11. Deletion of 2p: a cytogenetic and clinical update.
    Neidich J, Zackai E, Aronson M, Emanuel BS.
    Am J Med Genet; 1987 Jul; 27(3):707-10. PubMed ID: 3477100
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  • 13. 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 Jul; 35(4):208-12. PubMed ID: 1296516
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  • 16. 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
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  • 18. Duplication 11 (q21 to 23 leads to qter) syndrome.
    Francke U, Weber F, Sparkes RS, Mattson PD, Mann J.
    Birth Defects Orig Artic Ser; 1977 Oct; 13(3B):167-86. PubMed ID: 890090
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  • 19. Distal monosomy of the long arm of chromosome 6 (6q25----6qter) inherited by maternal translocation t(6q;17q).
    Oliveira-Duarte MH, Martelli-Soares LR, Sarquis-Cintra T, Machado ML, Lison MP.
    Ann Genet; 1990 Oct; 33(1):56-9. PubMed ID: 2195984
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  • 20. [Tetrasomy of the short arm of human chromosome 18: cytogenetics and phenotypic disorders].
    Kuleshov NP, Zaletaev DV, Levina LIa, Dement'eva GM, Arbuzov SP.
    Tsitol Genet; 1985 Oct; 19(6):452-6. PubMed ID: 4089954
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