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Journal Abstract Search

234 related items for PubMed ID: 1080041

  • 1. [Mosaic 14 trisomy in a female child with multiple abnormalities].
    Rethoré MO, Couturier J, Carpentier S, Ferrand J, Lejeune J.
    Ann Genet; 1975 Mar; 18(1):71-4. PubMed ID: 1080041
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  • 2. [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)].
    Turleau C, Rethoré MO, Junien C, Lejeune J, de Grouchy J.
    Ann Genet; 1979 Mar; 22(3):178-81. PubMed ID: 316677
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  • 3. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
    Raoul O, Rethoré MO, Dutriliaux B, Michon L, Lejeune J.
    Ann Genet; 1975 Mar; 18(1):35-9. PubMed ID: 1080036
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  • 4. [Mosaic trisomy 13 with isochromosome: 46, XX-46, XX, 13-, 13 q:].
    Emberger JM, Nègre C, Lafon R.
    Ann Genet; 1972 Jun; 15(2):111-4. PubMed ID: 4537722
    [No Abstract] [Full Text] [Related]

  • 5. Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?
    Shashi V, Golden WL, von Kap-Herr C, Wilson WG.
    Am J Med Genet; 1996 Mar 01; 62(1):38-41. PubMed ID: 8779322
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  • 7. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP, Kleczkowska A, Jaeken J, Van Herck K, Van den Berghe MH.
    Ann Genet; 1989 Mar 01; 32(3):177-9. PubMed ID: 2486064
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  • 8. Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant.
    Milunsky JM, Wyandt HE, Huang XL, Kang XZ, Elias ER, Milunsky A.
    Am J Med Genet; 1996 Jan 22; 61(3):269-73. PubMed ID: 8741873
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  • 9. Dermatoglyphics in children suffering from congenital defects, with and without chromosomal aberrations.
    Usoev SS.
    Sov Genet; 1974 Jul 15; 8(7):929-31. PubMed ID: 4278489
    [No Abstract] [Full Text] [Related]

  • 10. Secondary trisomy or mosaic "tetrasomy" 8p.
    Robinow M, Haney N, Chen H, Sorauf T, Van Dyke DL, Babu VR, Powell S, Maliszewski W, Guerin S, Landers JW.
    Am J Med Genet; 1989 Mar 15; 32(3):320-4. PubMed ID: 2729351
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  • 13. Unusual chromosomal mosaic (46, XX-46, XX, Cp+) in a girl with multiple malformations.
    Eriksson B, Fraccaro M, Hultén M, Lindsten J, Tiepolo L.
    Ann Genet; 1968 Mar 15; 11(1):6-10. PubMed ID: 5301761
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  • 14. 46,X,i(Xq)/47,XX,+13 mosaicism.
    Igarashi M, Tsukahara M, Sugio Y, Katayama K, Kajii T.
    Ann Genet; 1985 Mar 15; 28(4):241-4. PubMed ID: 3879438
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  • 15. [Partial 7q trisomy].
    Serville F, Broustet A, Sandler B, Bourdeau MJ, Leloup M.
    Ann Genet; 1975 Mar 15; 18(1):67-70. PubMed ID: 1080040
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  • 17. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA, Mikel'saar AV, Mikel'saar RV.
    Sov Genet; 1974 Jun 01; 8(5):651-7. PubMed ID: 4413436
    [No Abstract] [Full Text] [Related]

  • 18. [Trisomy of the chromosome 13 in a child with multiple malformations].
    Adámek R, Kaspárková Z, Kaláb Z, Bílek O, Sekanina Z, Frána L.
    Cesk Pediatr; 1974 Jan 01; 29(1):49-51. PubMed ID: 4452141
    [No Abstract] [Full Text] [Related]

  • 19. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
    Hartmann A, Hofmann UB, Hoehn H, Broecker EB, Hamm H.
    Pediatr Dermatol; 2004 Jan 01; 21(6):636-41. PubMed ID: 15575846
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