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Journal Abstract Search

254 related items for PubMed ID: 1684352

  • 1. 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
    [No Abstract] [Full Text] [Related]

  • 2. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS, Gibson L, McGrath J, Meyn MS, Breg WR, Yang-Feng TL.
    Am J Med Genet; 1993 May 15; 46(3):288-92. PubMed ID: 8488873
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  • 3. [Case of chromosome X pentasomy].
    Sito A, Krzyzanowska J, Hofman H, Witkowska J, Sioch R, Mroczek-Orłow T.
    Pediatr Pol; 1980 Jan 15; 55(1):77-80. PubMed ID: 7367071
    [No Abstract] [Full Text] [Related]

  • 4. [Importance of chromosomal satellites].
    Rosenkranz W, Glatzl J, Holzer S.
    Wien Klin Wochenschr; 1972 Nov 10; 84(45):725-7. PubMed ID: 4404500
    [No Abstract] [Full Text] [Related]

  • 5. [Interstitial deletion of the long arm of one 11 chromosome].
    Taillemite JL, Morlier BG, Roux C.
    Ann Genet; 1975 Mar 10; 18(1):61-3. PubMed ID: 1080039
    [Abstract] [Full Text] [Related]

  • 6. 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 Mar 10; 4(3):279-86. PubMed ID: 574719
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  • 9. [Monosomy of chromosome 21].
    Rogóyski A, Babel M, Tronowska TD.
    Pediatr Pol; 1983 Jun 10; 58(6):557-9. PubMed ID: 6646915
    [No Abstract] [Full Text] [Related]

  • 10. Tetrasomy 9p caused by idic (9) (pter----q13----pter).
    Cavalcanti DP, Ferrari I, de Almeida JC, de Pina Neto JM, de Oliveira JA.
    Am J Med Genet; 1987 Jul 10; 27(3):497-503. PubMed ID: 3631125
    [Abstract] [Full Text] [Related]

  • 11. [Complex rearrangement of chromosomes 3 and 5 in an adolescent with multiple abnormalities].
    Naffah J, Der Kaloustian V.
    Ann Genet; 1975 Jun 10; 18(2):121-4. PubMed ID: 242250
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  • 14. [Chromosome 8 trisomy in an infant].
    Rogóyski A, Babel M, Tronowska TD.
    Pediatr Pol; 1982 Jun 10; 57(5-6):425-7. PubMed ID: 7155694
    [No Abstract] [Full Text] [Related]

  • 15. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO, Karauzum SB, Mihci E, Tacoy S, Luleci G.
    Genet Couns; 2005 Jun 10; 16(2):129-38. PubMed ID: 16080292
    [Abstract] [Full Text] [Related]

  • 16. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
    Voss R, Lerer I, Maftzir G, Sheinis M, Cohen MM.
    Am J Med Genet; 1982 Jun 10; 12(2):131-9. PubMed ID: 7102721
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  • 18. Choanal atresia in a patient with the deletion (9p) syndrome.
    Shashi V, Golden WL, Fryburg JS.
    Am J Med Genet; 1994 Jan 01; 49(1):88-90. PubMed ID: 8172257
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  • 19. Isochromosome-formation in chromosome 9.
    Miller K, Arslan-Kirchner M.
    Ann Genet; 1994 Jan 01; 37(2):78-81. PubMed ID: 7985983
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