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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

236 related items for PubMed ID: 5314291

  • 1. [The Dr syndrome. Study of a further case (46, XX, 14r)].
    Gilgenkrantz S, Cabrol C, Lausecker C, Hartleyb ME, Bohe B.
    Ann Genet; 1971 Mar; 14(1):23-31. PubMed ID: 5314291
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  • 4. Ring 13 chromosome associated with microcephaly, congenital heart defect, intrauterine growth retardation, and abnormal skin pigmentation.
    Lowry RB, Dill FJ.
    Birth Defects Orig Artic Ser; 1977 Mar; 13(3B):216-22. PubMed ID: 890095
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  • 5. [Trial classification of D group chromosome long arm deletions. Apropos of a 15q- case].
    Laurent C, Noel B, David M.
    Ann Genet; 1971 Mar; 14(1):33-40. PubMed ID: 5314292
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  • 6. An infant with 45 chromosomes including a D-E (13-15-17-18) translocation chromosome.
    Borgaonkar DS, Mules E, Scott CI.
    Johns Hopkins Med J; 1971 May; 128(5):282-8. PubMed ID: 5556542
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  • 12. [Clinical diagnosis of the phenotype corresponding to a ring-shaped D chromosome].
    Rethoré MO, Praud E, Le Loc'h J, Joly C, Saraux H, Aussannaire M, Lejeune J.
    Presse Med (1893); 1970 Apr 25; 78(21):955-8. PubMed ID: 4986088
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  • 14. [Study of a 46,XX-46,XX,17r mosaicism].
    Petit P, Koulischer L.
    Ann Genet; 1971 Mar 25; 14(1):55-8. PubMed ID: 5314296
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  • 15. The 18p- syndrome. Report of two cases.
    Jacobsen P, Mikkelsen M.
    Ann Genet; 1968 Dec 25; 11(4):211-6. PubMed ID: 5306362
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  • 17. [A short arm deletion of chromosome 13].
    Emerit I, de Grouchy J, German J.
    Ann Genet; 1968 Sep 25; 11(3):184-6. PubMed ID: 5304619
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