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Journal Abstract Search

97 related items for PubMed ID: 13894418

  • 1. A male with XXXXY sex chromosomes.
    FRACCARO M, KLINGER HP, SCHUTT W.
    Cytogenetics; 1962; 1():53-63. PubMed ID: 13894418
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  • 5. Chromosomal anomalies in cryptorchidism and hypospadias.
    Yamaguchi T, Kitada S, Osada Y.
    Urol Int; 1991; 47(2):60-3. PubMed ID: 1686509
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  • 10. Chromosomal translocation in a mentally deficient child with cryptorchidism.
    BUHLER EM, ROSSIER R, BODIS I, VULLIET V, BUHLER UK, STALDER G.
    Acta Paediatr (Stockh); 1963 Mar; 52():177-82. PubMed ID: 14041555
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  • 11. Sex chromosome pentasomy 49,XXXXY connected with hypothyroidism. Case report.
    Wikiera B, Głab E, Slezak R, Wójcik E, Noczyńska A.
    Pediatr Endocrinol Diabetes Metab; 2009 Mar; 15(2):125-7. PubMed ID: 19772821
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  • 12. Caudal appendage, short terminal phalanges, deafness, cryptorchidism and mental retardation: a new syndrome?
    Lynch SA, Lee SG, Murday VA.
    Clin Dysmorphol; 1994 Oct; 3(4):340-6. PubMed ID: 7894739
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  • 13. Editorial: Genetics and mental retardation.
    Br Med J; 1975 Apr 12; 2(5962):55-6. PubMed ID: 1131544
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  • 15. 49 XXXXY syndrome with profound mental deficiency.
    Christodorescu D, Constantinescu E, Ciovîrnache M, Costiner E.
    Neurol Psychiatr (Bucur); 1978 Apr 12; 16(2):79-84. PubMed ID: 684348
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  • 16. Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly.
    Chen CP, Lin SP, Chen MR, Su JW, Chern SR, Chen YJ, Lee MS, Wang W.
    Genet Couns; 2012 Apr 12; 23(2):195-200. PubMed ID: 22876577
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  • 18. Letter: Sex-linked mental retardation.
    Gerrard JW, Renpenning HJ.
    Lancet; 1974 Jun 29; 1(7870):1346. PubMed ID: 4134321
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  • 19. A self-perpetuating ring chromosome.
    TURNER B, JENNINGS AN, den DULK GM, STAPLETON T.
    Med J Aust; 1962 Jul 14; 49(2)():56-8. PubMed ID: 13923190
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  • 20. Marker X chromosomes and mental retardation.
    Sutherland GR.
    N Engl J Med; 1977 Jun 16; 296(24):1415. PubMed ID: 859555
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