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Journal Abstract Search

277 related items for PubMed ID: 3789004

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  • 3. A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2.
    Ramer JC, Ladda RL, Frankel CA, Beckford A.
    Am J Med Genet; 1989 Mar; 32(3):359-63. PubMed ID: 2658585
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  • 5. 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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  • 7. 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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  • 11. Infantile hemangioendothelioma of the liver in patient with interstitial deletion of chromosome 6q: report of an autopsy case.
    Ito H, Yamasaki T, Okamoto O, Tahara E.
    Am J Med Genet; 1989 Nov 15; 34(3):325-9. PubMed ID: 2596522
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  • 12. Chromosome 10qter deletion syndrome: a review and report of three new cases.
    Wulfsberg EA, Weaver RP, Cunniff CM, Jones MC, Jones KL.
    Am J Med Genet; 1989 Mar 15; 32(3):364-7. PubMed ID: 2658586
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  • 14. Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newborns.
    Fryns JP, Kleczkowska A, Limbos C, Vandecasseye W, Van den Berghe H.
    Ann Genet; 1985 Mar 15; 28(4):248-50. PubMed ID: 3879440
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  • 16. Double chromosome anomaly: interstitial deletion 5q and reciprocal translocation (1;11)(p22;q21).
    de Michelena MI, Villacorta J, Chávez J.
    Am J Med Genet; 1990 May 15; 36(1):29-32. PubMed ID: 2185634
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  • 18. Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].
    Chitayat D, Babul R, Silver MM, Jay V, Teshima IE, Babyn P, Becker LE.
    Am J Med Genet; 1996 Jan 02; 61(1):45-8. PubMed ID: 8741917
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  • 19. Interstitial deletion of the long arm of chromosome 3.
    Martsolf JT, Ray M.
    Ann Genet; 1983 Jan 02; 26(2):98-9. PubMed ID: 6604494
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  • 20. Girl with accelerated growth, hearing loss, inner ear anomalies, delayed myelination of the brain, and del(22)(q13.1q13.2).
    Fujita Y, Mochizuki D, Mori Y, Nakamoto N, Kobayashi M, Omi K, Kodama H, Yanagawa Y, Abe T, Tsuzuku T, Yamanouchi Y, Takano T.
    Am J Med Genet; 2000 May 29; 92(3):195-9. PubMed ID: 10817654
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