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Journal Abstract Search

98 related items for PubMed ID: 7015155

  • 1.
    ; . PubMed ID:
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  • 2. [Cytogenetics of malignant hemopathies].
    Jotterand Bellomo M, Mühlematter D, Parlier V.
    Rev Med Suisse Romande; 1993 Apr; 113(4):291-303. PubMed ID: 8502884
    [No Abstract] [Full Text] [Related]

  • 3. [Chromosome analysis].
    Oosterwijk JC.
    TVZ; 1988 Jul 07; 42(14):462-5. PubMed ID: 3138786
    [No Abstract] [Full Text] [Related]

  • 4. [Indications of chromosome and DNA analysis for the diagnosis of genetic diseases].
    Romana SP, Gérard B.
    Rev Prat; 1997 Jun 01; 47(11):1241-52. PubMed ID: 9238821
    [No Abstract] [Full Text] [Related]

  • 5. [Discussion of the technical bases of pathology associated with chromosome anomalies. Discussion of their importance and significance in tumor processes].
    Zachar D.
    Arch Anat Cytol Pathol; 1985 Jun 01; 33(2):116-9. PubMed ID: 3890776
    [No Abstract] [Full Text] [Related]

  • 6. Chromosome analysis of human preimplantation embryos.
    Carrera M, Veiga A.
    Croat Med J; 1998 Jun 01; 39(2):121-7. PubMed ID: 9575266
    [Abstract] [Full Text] [Related]

  • 7. [Cytogenetic study of 500 patients selected in the research for chromosomal anomalies].
    Chaabouni H, Meddeb M, Buresi C, Ben Jemaa L.
    Tunis Med; 1992 Jan 01; 70(1):39-43. PubMed ID: 1570651
    [No Abstract] [Full Text] [Related]

  • 8. [Morphologic anomalies of the chromosomes of the 16th pair and the acoustic apparatus].
    Grimaud R, Gilgenkrantz S, Bemol P.
    Acta Otolaryngol; 1967 Jan 01; 63(2):144-8. PubMed ID: 6032378
    [No Abstract] [Full Text] [Related]

  • 9. [Genetic prognosis of chromosome translocations].
    Srsen S, Volna J.
    Cesk Pediatr; 1980 Apr 01; 35(4):196-203. PubMed ID: 7397898
    [No Abstract] [Full Text] [Related]

  • 10. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
    Voss R, Lerer I, Maftzir G, Sheinis M, Cohen MM.
    Am J Med Genet; 1982 Jun 01; 12(2):131-9. PubMed ID: 7102721
    [Abstract] [Full Text] [Related]

  • 11. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS, Hegmann K, Smith JL, Shaffer LG.
    Am J Med Genet; 1995 May 22; 57(1):31-4. PubMed ID: 7645595
    [Abstract] [Full Text] [Related]

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  • 13.
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  • 14. Autosomal imbalance syndromes: genetic interactions and the origin of congenital malformations in aneuploidy syndromes.
    Lurie IW.
    Am J Med Genet; 1993 Sep 01; 47(3):410-6. PubMed ID: 8135290
    [Abstract] [Full Text] [Related]

  • 15.
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  • 17. [Cytogenetics in pediatric practice. Experience of 10 years (author's transl)].
    Carnevale A, Blanco B, Frías S, Castillo J, Vázquez V.
    Rev Invest Clin; 1981 Sep 01; 33(2):175-81. PubMed ID: 7291763
    [No Abstract] [Full Text] [Related]

  • 18. [Terminology and principal factors studied in genetics].
    Cordier MP.
    Soins; 1983 Apr 01; (403):9-10. PubMed ID: 6346506
    [No Abstract] [Full Text] [Related]

  • 19. [Detection of submicroscopic chromosome abnormalities by comparative genomic hybridization].
    Kirchhoff M, Rose H, Gerdes T, Lundsteen C.
    Ugeskr Laeger; 2001 Oct 08; 163(41):5652-7. PubMed ID: 11665466
    [Abstract] [Full Text] [Related]

  • 20. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov 08; 15(5):469-73. PubMed ID: 7332149
    [Abstract] [Full Text] [Related]

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