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Journal Abstract Search

80 related items for PubMed ID: 4133844

  • 1.
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  • 3. [Trisomy 18 and esophageal diverticulum].
    Bottriaux M, De Leener L, Bersou H.
    Acta Paediatr Belg; 1973; 27(1):13-20. PubMed ID: 4200159
    [No Abstract] [Full Text] [Related]

  • 4. [Phenocopy of trisomy 18].
    Hongre JF, Toursei F, Staquet MF, Farriaux JP, Walbaum R.
    Ann Pediatr (Paris); 1972 Nov 02; 19(11):825-30. PubMed ID: 4641249
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  • 5. [A case of double trisomy: 48,XXX,18+].
    Emberger JM, Sarran R, Balzing P.
    Ann Genet; 1971 Dec 02; 14(4):301-3. PubMed ID: 5316134
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  • 8. 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 02; 10(4):159-66. PubMed ID: 5301688
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  • 9. The Edwards-Smith syndrome in a newborn girl.
    Guschina LA, Petrova SP, Bokarius LV.
    Sov Genet; 1974 Oct 01; 8(11):1471-2. PubMed ID: 4445910
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  • 10. [Chromosome 18 trisomy syndrome].
    Badalian LO, Zhurba LG, Koroleva IA, Aĭngorn ED, Veshneva IV.
    Pediatriia; 1972 Mar 01; 51(3):56-9. PubMed ID: 5014690
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  • 11. Double trisomy 48,XXX,+ 18 in a newborn.
    Rosenfeld W, Verma RS, Jhaveri RC, Salazar D, Dosik H.
    Am J Med Genet; 1981 Mar 01; 8(1):67-71. PubMed ID: 7246607
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  • 12. [Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)].
    Rethoré MO, Lafourcade J, Couturier J, Harpey JP, Hamet M, Engler R, Alcindor LG, Lejeune J.
    Ann Genet; 1982 Mar 01; 25(1):36-42. PubMed ID: 6979298
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  • 13. [Trisomy 18 and its dermatoglyphic diagnosis].
    Walbaum R, Farriaux JP, Breynaert R, Fontaine G.
    Ann Pediatr (Paris); 1966 Dec 02; 13(12):794-803. PubMed ID: 5990122
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  • 14. Multiple anomalies associated with an extra small metacentric chromosome: modified Giemsa stain results.
    Tangheroni W, Cao A, Furbetta M.
    Humangenetik; 1973 Dec 02; 18(4):291-5. PubMed ID: 4125989
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  • 15. Clinical aspects of chromosome aberrations.
    Dutrillaux B, Lejeune J.
    Triangle; 1972 Dec 02; 11(3):81-9. PubMed ID: 4656754
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  • 16. [Clinical anatomic and histopathological study of ocular signs in 2 cases of mosaicism associated with autosomal 18-21 double trisomy].
    Laliam M, Laliam N, Ouadahi MS, Iles S, Ould Larbi L.
    Bull Mem Soc Fr Ophtalmol; 1972 Dec 02; 85(0):83-90. PubMed ID: 4211332
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  • 17. [Phenocopy of trisomy 18: an autosomal recessive disease? (author's transl)].
    Le Marec B, Paty E, Roussey M, Walbaum R, Cadoret G, Houdeau M, Picard F, Senecal J.
    Arch Fr Pediatr; 1981 Apr 02; 38(4):253-9. PubMed ID: 7294952
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  • 18. [On three cases of C trisomy].
    Lejeune J, Dutrillaux B, Rethoré MO, Berger R, Debray H, Veron P, Gorce F, Grossiord A.
    Ann Genet; 1969 Mar 02; 12(1):28-35. PubMed ID: 5306709
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  • 20. [Trisomy due to transmitted translocation t(13 q , 14 q ). Estimation of recurrence risks].
    Belaisch G, Despres P, Plainfosse B, Rethore O, Emerit I, Loewe-Lyon S, Lejeune J, Seringe P.
    Arch Fr Pediatr; 1971 Oct 02; 28(8):865-74. PubMed ID: 5123542
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