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Journal Abstract Search

290 related items for PubMed ID: 5306714

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  • 3. An infant with double trisomy (48,XXX, + 18).
    Jaruratanasirikul S, Jinorose U.
    Am J Med Genet; 1994 Jan 15; 49(2):207-10. PubMed ID: 8116670
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  • 4. [Apropos of trisomy 18 - a study of 4 observations].
    Gilgenkrantz S, Sapelier J, Thiriet M, Kahn C, Pierson M.
    Ann Genet; 1967 Mar 15; 10(1):32-8. PubMed ID: 5300124
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  • 6. [A case of double trisomy: 48,XXX,18+].
    Emberger JM, Sarran R, Balzing P.
    Ann Genet; 1971 Dec 15; 14(4):301-3. PubMed ID: 5316134
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  • 8. [Peculiarities of dermatoglyphics in chromosomal diseases].
    Verlinskaia DK, Shtil'bans II.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1966 Dec 15; 66(11):1608-13. PubMed ID: 4234112
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  • 10. Partial trisomy for different segments of chromosome 13 in several individuals of the same family.
    Wilroy RS, Summitt RL, Martens PR.
    Birth Defects Orig Artic Ser; 1975 Dec 15; 11(5):217-22. PubMed ID: 1218217
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  • 11. 49,XXYY, +18 in a liveborn male.
    Webb GC, Krumins EJ, Leversha MA, Ford GW.
    J Med Genet; 1984 Jun 15; 21(3):232. PubMed ID: 6748025
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  • 12. A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.
    Valdmanis A, Pearson G, Siegel AE, Hoeksema RH, Mann JD.
    Ann Genet; 1967 Dec 15; 10(4):159-66. PubMed ID: 5301688
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  • 15. [The importance of configurations or papillary lines in the identification of chromosomal diseases].
    Rott HD.
    Folia Clin Int (Barc); 1969 Oct 15; 19(10):500-6. PubMed ID: 5396731
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  • 17. Neurological disorders in patients with chromosomal anomalies.
    Kunze J.
    Neuropediatrics; 1980 Aug 15; 11(3):203-49. PubMed ID: 6999382
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  • 20. [Polymalformation syndrome caused by 13 then 21 trisomy in 2 children of the same sibship].
    Colette C, Maire P.
    Bull Fed Soc Gynecol Obstet Lang Fr; 1970 Aug 15; 22(2):224-5. PubMed ID: 5474564
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