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PUBMED FOR HANDHELDS

Journal Abstract Search


188 related items for PubMed ID: 555637

  • 1. [9p monosomy. About a new case. Clinical and cytogenetic study (author's transl)].
    Lajarrige C, Bouquier JJ, Ronayette D, Tchertoff C, Faugeras C, Barthe D, Laleu J.
    Ann Pediatr (Paris); 1979 Nov; 26(9):631-6. PubMed ID: 555637
    [No Abstract] [Full Text] [Related]

  • 2. [12 p trisomy. A new case (author's transl)].
    Kubryk N, Prieur M, Borde M.
    Ann Pediatr (Paris); 1980 Dec; 27(10):695-9. PubMed ID: 7212558
    [No Abstract] [Full Text] [Related]

  • 3. [Two new cases of partial monosomy 11q with breakpoint in 11q24 (author's transl)].
    Laurent C, Biemont MC, Veyron M, Guilhot J, Guibaud P.
    Ann Genet; 1979 Dec; 22(4):239-41. PubMed ID: 317789
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  • 6. [De novo monosomy 4q32.1 leads to 4qter in a newborn with multiple malformations (author's transl)].
    Rethoré MO, Couturier J, Mselati JC, Cochois B, Lavaud J, Lejeune J.
    Ann Genet; 1979 Dec; 22(4):214-6. PubMed ID: 317783
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  • 7. [Monosomy 7qter (author's transl)].
    Turleau C, de Grouchy J, Perignon F, Lenoir G.
    Ann Genet; 1979 Dec; 22(4):242-4. PubMed ID: 317790
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  • 10. Cri du chat-syndrome in combination with partial trisomy 9 p.
    Sigmund J, Frisch H, Heinz-Erian P, Rhomberg K, Wegner RD.
    Padiatr Padol; 1986 Dec; 21(1):61-7. PubMed ID: 3960564
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  • 11. [Trisomy 9p - clinical and cytogenetic syndrome].
    Hitrec V, Zergollern L.
    Acta Med Iugosl; 1979 Dec; 33(2):169-82. PubMed ID: 506795
    [No Abstract] [Full Text] [Related]

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  • 13. [9p syndrome. Deletion of the short arm of chromosome 9; Monosomy of short arm 9].
    Nielsen J, Christiansen F, Homma A, Rasmussen K.
    Ugeskr Laeger; 1977 Jan; 139(4):204. PubMed ID: 835175
    [No Abstract] [Full Text] [Related]

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  • 15. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat].
    Di Cesare D, Paludetto R, Casullo C, Pagano L, Stabile M, Sicolo A, Ventruto V.
    Minerva Pediatr; 1980 Dec 15; 32(23):1349-52. PubMed ID: 7219376
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  • 18. Partial monosomy 10p syndrome.
    Koenig R, Kessel E, Schoenberger W.
    Ann Genet; 1985 Dec 15; 28(3):173-6. PubMed ID: 3879152
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  • 19. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov 15; 15(5):469-73. PubMed ID: 7332149
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  • 20. [Tetrasomy 9p].
    Foerster W, Koch M, Hansen S.
    Monatsschr Kinderheilkd; 1985 Sep 15; 133(9):694-7. PubMed ID: 2865673
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