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Journal Abstract Search

168 related items for PubMed ID: 1481806

  • 1. Interstitial deletion of the short arm of chromosome 1 (46XY, del(1)(p13p22.3)).
    Mattia FR, Wardinsky TD, Tuttle DJ, Grix A, Smith KA, Walling P.
    Am J Med Genet; 1992 Nov 15; 44(5):551-4. PubMed ID: 1481806
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  • 2. A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome.
    Gorski JL, Uhlmann WR, Glover TW.
    Am J Med Genet; 1990 Dec 15; 37(4):471-4. PubMed ID: 2260590
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  • 7. Unique de novo interstitial deletion of chromosome 17, del(17) (q23.2q24.3) in a female newborn with multiple congenital anomalies.
    Levin ML, Shaffer LG, Lewis RAp6, Gresik MV, Lupski JR.
    Am J Med Genet; 1995 Jan 02; 55(1):30-2. PubMed ID: 7702093
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  • 8. [Del(1)(q22-q25) syndrome. Cytogenetics and phenotype].
    Zaletaev DV, Dadali EL, Kuleshov NP.
    Tsitol Genet; 1987 Jan 02; 21(3):213-6. PubMed ID: 3617217
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  • 9. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4.
    Beall MH, Falk RE, Ying KL.
    Am J Med Genet; 1988 Nov 02; 31(3):553-7. PubMed ID: 3067576
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  • 11. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
    Galasso C, Lo-Castro A, Lalli C, Nardone AM, Gullotta F, Curatolo P.
    J Child Neurol; 2008 Jul 02; 23(7):802-6. PubMed ID: 18658079
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  • 12. Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2.
    Saal HM, King LJ, Zimmerman D, Johnson RC, Carr AG, Samango-Sprouse CA, Stanley W.
    Am J Med Genet; 1996 Dec 30; 66(4):373-7. PubMed ID: 8989454
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  • 16. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
    Meng J, Fujita H, Nagahara N, Kashiwai A, Yoshioka Y, Funato M.
    Am J Med Genet; 1992 Jul 01; 43(4):747-50. PubMed ID: 1621768
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  • 19. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
    Davies J, Voullaire L, Bankier A.
    Ann Genet; 1990 Jul 01; 33(2):92-5. PubMed ID: 2241091
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  • 20. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
    Lin AE, Garver KL, Diggans G, Clemens M, Wenger SL, Steele MW, Jones MC, Israel J.
    Am J Med Genet; 1988 Nov 01; 31(3):533-48. PubMed ID: 3067575
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