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Journal Abstract Search

118 related items for PubMed ID: 3379382

  • 1. [A difficult cytogenetic diagnosis of 4p monosomy].
    Vittu G, Croquette MF, Boidein F, Cousin J.
    J Genet Hum; 1988 Jan; 36(1-2):75-82. PubMed ID: 3379382
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  • 2. Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32----qter.
    Al-Awadi SA, Teebi AS, Sundareshan TS.
    Ann Genet; 1985 Jan; 28(3):181-4. PubMed ID: 3879154
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  • 6. Multiple critical smallest region of overlap in monosomy 16Q syndrome?
    Doco-Fenzy M, Elchardus JF, Brami G, Digeon B, Gruson N, Adnet JJ.
    Genet Couns; 1994 Jan; 5(1):39-44. PubMed ID: 8031534
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  • 11. A case of Alagille's syndrome with translocation (4;14) (q21;q21).
    Mujica P, Morali A, Vidailhet M, Pierson M, Gilgenkrantz S.
    Ann Genet; 1989 Jan; 32(2):117-9. PubMed ID: 2757361
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  • 14. Monosomy 13q32.3----qter: report of two cases.
    Rivera H, González-Flores SA, Rivas F, Sánchez-Corona J, Moller M, Cantú JM.
    J Med Genet; 1985 Apr; 22(2):142-5. PubMed ID: 3989831
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  • 17. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J, Kimijima Y, Yamada S, Amagasa T, Saito-Ohara F.
    J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
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  • 18. Molecular cytogenetic analysis of de novo partial monosomy 4p (4p16.2-->pter) and partial trisomy 8p (8p23.2-->pter).
    Chen CP, Lin SP, Chern SR, Lee CC, Chen LF, Chen YJ, Wang W.
    Genet Couns; 2006 Jun; 17(1):81-5. PubMed ID: 16719283
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  • 19. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
    Wouters CH, van Bodegom TM, Moll HA, Govaerts LC.
    Ann Genet; 1999 Jun; 42(3):160-5. PubMed ID: 10526659
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  • 20. Monosomy 8p: an easily overlooked syndrome.
    Bröcker-Vriends AH, Mooij PD, van Bel F, Beverstock GC, van de Kamp JJ.
    J Med Genet; 1986 Apr; 23(2):153-4. PubMed ID: 3712390
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