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PUBMED FOR HANDHELDS

Journal Abstract Search

132 related items for PubMed ID: 738724

  • 41.
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  • 44. A case of distal 4q trisomy due to familial (4;5)(q31;p15) translocation.
    Oka S, Nakagome Y, Honda T, Arima M.
    Jinrui Idengaku Zasshi; 1978 Jun; 23(2):167-72. PubMed ID: 691839
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  • 45. Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literature.
    Berner AL, Bağci S, Wohlleber E, Engels E, Müller A, Bartmann P, Weber RG, Reutter H.
    Cytogenet Genome Res; 2012 Jun; 136(4):308-13. PubMed ID: 22433391
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  • 48. Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?
    Breuning MH, Bijlsma JB, de France HF.
    Hum Genet; 1977 Aug 31; 38(1):7-13. PubMed ID: 903156
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  • 49. Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20.
    Palmer CG, Poland C, Reed T, Kojetin J.
    Hum Genet; 1976 Feb 29; 31(2):219-25. PubMed ID: 1248831
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  • 50. Severe mental retardation in a boy with partial trisomy 10q and partial monosomy 2q.
    Sills JA, Buckton KE, Raeburn JA.
    J Med Genet; 1976 Dec 29; 13(6):507-10. PubMed ID: 1018309
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  • 53. Partial trisomy 2q.
    Schumacher RE, Rocchini AP, Wilson GN.
    Clin Genet; 1983 Mar 29; 23(3):191-4. PubMed ID: 6851215
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  • 55. Duplication (partial trisomy) of the distal long arm of chromosome 17: a new clinically recognizable chromosome disorder.
    Berberich MS, Carey JC, Lawce HJ, Hall BD.
    Birth Defects Orig Artic Ser; 1978 Mar 29; 14(6C):287-95. PubMed ID: 728583
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  • 57. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to partial 1q duplication and possible 18p deletion: a study of four individuals in two families.
    Liberfarb RM, Breg WR, Atkins L, Holmes LB.
    Am J Med Genet; 1979 Mar 29; 4(1):27-37. PubMed ID: 495650
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  • 59. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.
    Verma RS, Dosik H, Wexler IB.
    J Genet Hum; 1977 Dec 29; 25(4):295-301. PubMed ID: 599332
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