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Journal Abstract Search

128 related items for PubMed ID: 6215610

  • 1. Higher incidence of small Y chromosome in humans with trisomy 21 (Down syndrome).
    Verma RS, Huq A, Madahar C, Qazi Q, Dosik H.
    Pediatr Res; 1982 Sep; 16(9):769-70. PubMed ID: 6215610
    [Abstract] [Full Text] [Related]

  • 2. Human chromosomal heteromorphisms in American blacks. VI. Higher incidence of longer Y owing to non-fluorescent (nf) segment.
    Verma RS, Evans-McCalla M, Dosik H.
    J Med Genet; 1982 Aug; 19(4):297-301. PubMed ID: 6889654
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  • 3. Nondisjunction.
    Ford CE.
    Hum Genet Suppl; 1981 Aug; 2():103-43. PubMed ID: 6218132
    [No Abstract] [Full Text] [Related]

  • 4. The origin of sex chromosome aneuploidy.
    Jacobs P, Hassold T, Harvey J, May K.
    Prog Clin Biol Res; 1989 Aug; 311():135-51. PubMed ID: 2528150
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  • 5. Inherited pericentric inversion of Y-chromosome with trisomy 21. A case report.
    Krishna Murthy DS, Murthy SK, Patel JK, Banker GN, Shah VC.
    Ann Genet; 1989 Aug; 32(1):47-51. PubMed ID: 2526612
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  • 6. Results of 538 chromosome studies on patients referred for cytogenetic analysis.
    Mulcahy MT, Jenkyn J.
    Med J Aust; 1972 Dec 09; 2(24):1333-8. PubMed ID: 4265391
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  • 12. Patient with Down's syndrome and male pseudohermaphroditism with a 47, XY, plus21 karyotype.
    Mello RS, Souza OA, Santos Mello EM, Pimentel EC.
    Clin Genet; 1974 Dec 09; 5(3):259-62. PubMed ID: 4275956
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  • 13. A cytogenetic survey of an institution for the mentally retarded: I. Chromosome abnormalities.
    Jacobs PA, Matsuura JS, Mayer M, Newlands IM.
    Clin Genet; 1978 Jan 09; 13(1):37-60. PubMed ID: 146575
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  • 18. Abnormal chromosome 22 and recurrence of trisomy-22 syndrome.
    Emanuel BS, Zackai EH, Aronson MM, Mellman WJ, Moorhead PS.
    J Med Genet; 1976 Dec 09; 13(6):501-6. PubMed ID: 138742
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