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Journal Abstract Search

141 related items for PubMed ID: 6862435

  • 21. Nonrandom chromosomal changes in retinoblastomas.
    Pogosianz HE, Kuznetsova LE.
    Arch Geschwulstforsch; 1986; 56(2):135-43. PubMed ID: 3707294
    [Abstract] [Full Text] [Related]

  • 22. Gene carrier detection in retinoblastoma.
    Gallie BL.
    Ophthalmology; 1980 Jun; 87(6):591-5. PubMed ID: 7413148
    [Abstract] [Full Text] [Related]

  • 23. Bleomycin-induced chromosomal aberrations and sister chromatid exchanges in Down lymphocyte cultures.
    Iijima K, Morimoto K, Koizumi A, Higurashi M, Hirayama M.
    Hum Genet; 1984 Jun; 66(1):57-61. PubMed ID: 6199286
    [Abstract] [Full Text] [Related]

  • 24. Genetic predisposition to retinoblastoma (Rb).
    Zheng Y, Tang D, Peng H.
    Yan Ke Xue Bao; 1993 Sep; 9(3):149-52, 125. PubMed ID: 8168611
    [No Abstract] [Full Text] [Related]

  • 25. Chromosome errors in retinoblastoma.
    Howard RO.
    Birth Defects Orig Artic Ser; 1982 Sep; 18(6):703-27. PubMed ID: 6756503
    [No Abstract] [Full Text] [Related]

  • 26. Localisation of 7-12-dimethylbenz(a)anthracene induced chromatid breaks and sister chromatid exchanges in chromosomes 1 and 2 of bone marrow cells of rat in vivo.
    van Kesteren-van Leeuwen AC, Natarajan AT.
    Chromosoma; 1980 Sep; 81(3):473-81. PubMed ID: 6778675
    [Abstract] [Full Text] [Related]

  • 27. Chiasma derived genetic maps and recombination fractions: chromosome 13 with reference to the proposed 13q14 retinoblastoma locus.
    Palmer RW, Hultén MA.
    J Med Genet; 1982 Apr; 19(2):125-9. PubMed ID: 6951998
    [Abstract] [Full Text] [Related]

  • 28. Analysis of a BrdU-sensitive site in the cactus mouse (Peromyscus eremicus): chromosomal breakage and sister-chromatid exchange.
    Schneider NR, Chaganti RS, German J.
    Chromosoma; 1980 Apr; 77(3):379-89. PubMed ID: 7371461
    [Abstract] [Full Text] [Related]

  • 29. Sporadic bilateral retinoblastoma and 13q- chromosomal deletion.
    Francke U, Kung F.
    Med Pediatr Oncol; 1976 Apr; 2(4):379-85. PubMed ID: 1004381
    [Abstract] [Full Text] [Related]

  • 30. [Genetic predisposition to retinoblastoma(Rb)].
    Zheng YL.
    Zhonghua Yan Ke Za Zhi; 1992 Mar; 28(2):71-3. PubMed ID: 1425035
    [No Abstract] [Full Text] [Related]

  • 31. Retinoblastoma with 13q- chromosomal deletion associated with maternal paracentric inversion of 13q.
    Sparkes RS, Muller H, Klisak I.
    Science; 1979 Mar 09; 203(4384):1027-9. PubMed ID: 424728
    [Abstract] [Full Text] [Related]

  • 32. Chromosome aberrations and sister-chromatid exchanges (SCEs) in peripheral blood lymphocytes of patients suffering from poliomyelitis.
    Bhatnagar A, Rani R, Ghosh PK.
    Mutat Res; 1984 Sep 09; 141(1):55-8. PubMed ID: 6090893
    [Abstract] [Full Text] [Related]

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  • 36. Chromosomal anomalies in patients with retinoblastoma.
    Wilson MG, Ebbin AJ, Towner JW, Spencer WH.
    Clin Genet; 1977 Jul 09; 12(1):1-8. PubMed ID: 891004
    [Abstract] [Full Text] [Related]

  • 37. Retinoblastoma in association with the chromosome breakage syndromes Fanconi's anaemia and Bloom's syndrome: clinical and cytogenetic findings.
    Gibbons B, Scott D, Hungerford JL, Cheung KL, Harrison C, Attard-Montalto S, Evans M, Birch JM, Kingston JE.
    Clin Genet; 1995 Jun 09; 47(6):311-7. PubMed ID: 7554365
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