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Journal Abstract Search

189 related items for PubMed ID: 1080039

  • 1. [Interstitial deletion of the long arm of one 11 chromosome].
    Taillemite JL, Morlier BG, Roux C.
    Ann Genet; 1975 Mar; 18(1):61-3. PubMed ID: 1080039
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  • 2. Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases.
    Young RS, Weaver DD, Kukolich MK, Heerema NA, Palmer CG, Kawira EL, Bender HA.
    Am J Med Genet; 1984 Feb; 17(2):437-50. PubMed ID: 6199974
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  • 3. Monosomy 21: a possible stepwise evolution of the karyotype.
    Abeliovich D, Carmi R, Karplus M, Bar-Ziv J, Cohen MM.
    Am J Med Genet; 1979 Feb; 4(3):279-86. PubMed ID: 574719
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  • 4. 7q deletion syndrome (7q32 leads to 7qter).
    Harris EL, Wappner RS, Palmer CG, Hall B, Dinno N, Seashore MR, Breg WR.
    Clin Genet; 1977 Oct; 12(4):233-8. PubMed ID: 912940
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  • 6. 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
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  • 9. A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21-23 leads to 1q25.
    Taysi K, Sekhon GS, Hillman RE.
    Am J Med Genet; 1982 Dec; 13(4):423-30. PubMed ID: 7158642
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  • 11. [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].
    Turleau C, Grouchy J, Bocquentin F, Roubin M, Colin FC.
    Ann Genet; 1975 Mar; 18(1):41-4. PubMed ID: 1080037
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  • 14. Chromosome 6q- and associated malformations.
    Liberfarb RM, Atkins L, Holmes LB.
    Ann Genet; 1978 Dec; 21(4):223-5. PubMed ID: 314259
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  • 18. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
    Murthy DS, Murthy SK, Banker GJ, Patel AJ.
    Indian Pediatr; 1991 May; 28(5):546-9. PubMed ID: 1684352
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  • 20. Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case.
    Tenconi R, Baccichetti C, Anglani F, Pellergrino PA, Kaplan JC, Junien C.
    Ann Genet; 1975 Jun; 18(2):95-8. PubMed ID: 1081371
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