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Journal Abstract Search

191 related items for PubMed ID: 6228144

  • 1. Ring chromosome 21 in phenotypically apparently normal persons: report of two families from Switzerland and Italy.
    Schmid W, Tenconi R, Baccichetti C, Caufin D, Schinzel A.
    Am J Med Genet; 1983 Nov; 16(3):323-9. PubMed ID: 6228144
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  • 2. t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndrome.
    Dallapiccola B, Bianco I, Brinchi V, Santulli B, Scarano G, Sicolo A, Stabile M, Ventruto V.
    Ann Genet; 1982 Nov; 25(1):56-8. PubMed ID: 6211124
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  • 4. Down's syndrome associated with a familial (21q-; 22q+) translocation.
    Cohen MM, Davidson RG.
    Cytogenetics; 1967 Nov; 6(5):321-30. PubMed ID: 4231490
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  • 8. Down's syndrome at young maternal age; cytogenetical and genealogical study of eighty-two families.
    Mikkelson M.
    Ann Hum Genet; 1967 Aug; 31(1):51-69. PubMed ID: 4228454
    [No Abstract] [Full Text] [Related]

  • 9. A case of mosaic Down's syndrome with two Robertsonian translocations.
    Leal-Garza CH, Cortés-Gutiérrez EI, Ortiz-Jalomo R, García-Cavazos R.
    Rev Invest Clin; 1996 Aug; 48(5):385-8. PubMed ID: 8968157
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  • 10. Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son.
    Fryns JP, Kleczkowska A, Smeets E, Van Den Berghe H.
    Ann Genet; 1992 Aug; 35(2):121-3. PubMed ID: 1524410
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  • 11. Down's syndrome. A cytogenetic and clinical study of 134 patients with special reference to translocation cases.
    Zizka J.
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1972 Aug; 15(1):1-127. PubMed ID: 4264502
    [No Abstract] [Full Text] [Related]

  • 12. [Cytogenetic and dermatoglyphic studies in Down's syndrome with G-G translocation].
    Trebicka-Kwiatkowska B, Raczkiewicz B, Galińska I, Gasiorowski A.
    Pol Tyg Lek; 1973 Aug 06; 28(32):1220-2. PubMed ID: 4270748
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  • 13. A mother with Down's syndrome and her chromosomally normal infant.
    Reiss JA, Lovrien EW, Hecht F.
    Ann Genet; 1971 Sep 06; 14(3):225-7. PubMed ID: 4255605
    [No Abstract] [Full Text] [Related]

  • 14. [Transmission of an 18 ring chromosome in two generations in subjects of normal phenotype].
    Faugeras C, Barthe D.
    J Genet Hum; 1986 Aug 06; 34(3-4):313-20. PubMed ID: 3760834
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  • 15. Tandem duplication chromosome 21 in the offspring of a ring chromosome 21 carrier.
    Miller K, Reimer A, Schulze B.
    Ann Genet; 1987 Aug 06; 30(3):180-2. PubMed ID: 2960262
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  • 16. Down's syndrome and deletion of short arms of a G chromosome.
    Ballantyne GH, Parslow MI, Veale AM, Pullon DH.
    J Med Genet; 1977 Apr 06; 14(2):147-50. PubMed ID: 140219
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  • 17. Ring chromosome 6: case report and review.
    Nishi Y, Yoshimura O, Ohama K, Usui T.
    Am J Med Genet; 1982 May 06; 12(1):109-14. PubMed ID: 7091194
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  • 18. Familial Down's syndrome with G-G translocation.
    Hubner H, Jeske J, Dzida J.
    Pol Med Sci Hist Bull; 1969 Oct 06; 12(4):164-7. PubMed ID: 4257690
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  • 19. [Complete Down's syndrome in a boy, formed by chromosomic mosaicism 46-XY isochromosome 21 and 47-XY, trisomy 21 with mosaicism of the mother 46-XX and 47-XX, trisomy 21)].
    Raichs A, Tamparillas M.
    Sangre (Barc); 1967 Oct 06; 12(1):71-80. PubMed ID: 4235850
    [No Abstract] [Full Text] [Related]

  • 20. Cytogenetic studies in families with two 47, +21-siblings.
    Dhadial R, Pfeiffer RA.
    J Genet Hum; 1972 Dec 06; 20(4):297-322. PubMed ID: 4281439
    [No Abstract] [Full Text] [Related]

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