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Journal Abstract Search

171 related items for PubMed ID: 6982669

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  • 3. 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; 11(1):6-10. PubMed ID: 5301761
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  • 4. Ring 10 chromosome: 46,XX,r10(p15q26).
    Sparkes RS, Ling SM, Muller H.
    Hum Genet; 1978 Sep 19; 43(3):341-5. PubMed ID: 700708
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  • 5. [Ring chromosome 22. Description of a new case (1)].
    Gil Benso R, López Ginés C, Gregori Romero M, Galán Sánchez F, Pellín Pérez A.
    An Esp Pediatr; 1991 Jul 19; 35(1):62-4. PubMed ID: 1772175
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  • 6. Phenotype associated with ring 10 chromosome: report of patient and review of literature.
    Michels VV, Driscoll DJ, Ledbetter DH, Riccardi VM.
    Am J Med Genet; 1981 Jul 19; 9(3):231-7. PubMed ID: 7025632
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  • 7. [A case of translocation t(Cp-; Bp+)].
    Ricci N, Ventimiglia B, Dallapiccola B, Preto G.
    Ann Genet; 1967 Jun 19; 10(2):82-5. PubMed ID: 5298977
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  • 10. [Cp trisomy: a new syndrome].
    Canu JM, Buentello L, Armendares S.
    Ann Genet; 1971 Sep 19; 14(3):177-86. PubMed ID: 5315464
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  • 12. [Syndrome of congenital anomalies in a girl with karyotype 47,XXX].
    Kańska B, Kleczkowska A, Knaus A, Sokolowski J, Stapińska J.
    Pediatr Pol; 1971 Jan 19; 46(1):81-5. PubMed ID: 5545829
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  • 14. [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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