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Journal Abstract Search

138 related items for PubMed ID: 8689618

  • 21. [Hereditary tumors and chromosome aberrations with special reference to retinoblastoma].
    Sasaki MS.
    Gan To Kagaku Ryoho; 1986 Mar; 13(3 Pt 2):645-51. PubMed ID: 3963835
    [Abstract] [Full Text] [Related]

  • 22. High-resolution chromosome analysis in retinoblastoma.
    Toncheva D, Genkova P, Tzoneva M, Konstantinov I, Markova V.
    Neoplasma; 1987 Mar; 34(1):23-6. PubMed ID: 3561603
    [Abstract] [Full Text] [Related]

  • 23. Hereditary retinoblastoma and 13q--mosaicism.
    Dudin G, Nasr A, Traboulsi E, Khouri F, Der Kaloustian VM.
    Cytogenet Cell Genet; 1984 Mar; 38(3):235-7. PubMed ID: 6336322
    [Abstract] [Full Text] [Related]

  • 24. Detection by electron microscopy of a small subband 13q14.11 deletion in an hereditary retinoblastoma.
    Lemieux N, Messier PE, Drouin R, Jacob JL, Milot J, Richer CL.
    Cancer Genet Cytogenet; 1990 Sep; 48(2):265-9. PubMed ID: 2397457
    [Abstract] [Full Text] [Related]

  • 25. [Studies on deletions on chromosome 13 and their transmission in patients with retinoblastoma].
    Gao Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1991 Jun; 13(3):157-60. PubMed ID: 1831719
    [Abstract] [Full Text] [Related]

  • 26. Maternal origin of 47,XXY and confined placental mosaicism 47,XXY/48,XXY,+13 in an infant conceived through IVF.
    Wu EX, Wilson AD, Wong EC, Havelock JC, Ma S.
    J Assist Reprod Genet; 2013 Jun; 30(6):807-12. PubMed ID: 23624985
    [No Abstract] [Full Text] [Related]

  • 27. [Retinoblastoma: first case with a ring chromosome 13 in black Africa].
    Diallo JS, Afoutou JM, Balo K.
    Rev Int Trach Pathol Ocul Trop Subtrop Sante Publique; 1987 Jun; (64):183-6. PubMed ID: 3504037
    [No Abstract] [Full Text] [Related]

  • 28. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
    Mark HF, Bai H, Sotomayor E, Mark S, Zolnierz K, Airall E, Sigman M.
    Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
    [Abstract] [Full Text] [Related]

  • 29. Retinoblastoma and its association with a deletion in chromosome #13: a survey using high-resolution chromosome techniques.
    Johnson MP, Ramsay N, Cervenka J, Wang N.
    Cancer Genet Cytogenet; 1982 May; 6(1):29-37. PubMed ID: 7104985
    [Abstract] [Full Text] [Related]

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

  • 31. Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47,XXY, mosaic 46,XY/47,XXY and 47,XYY) assessed by fluorescence in-situ hybridization.
    Blanco J, Egozcue J, Vidal F.
    Hum Reprod; 2001 May; 16(5):887-92. PubMed ID: 11331634
    [Abstract] [Full Text] [Related]

  • 32. XY/XXY mosaicism and fragile X syndrome.
    Fryns JP, Kleczkowska A, Kubień E, Petit P, Haspeslagh M, Lindemans I, Van Den Berghe H.
    Ann Genet; 1983 May; 26(4):251-3. PubMed ID: 6607708
    [Abstract] [Full Text] [Related]

  • 33. [Genetic study of retinoblastoma].
    Sun YJ.
    Zhonghua Yan Ke Za Zhi; 1989 May; 25(3):152-5. PubMed ID: 2582950
    [Abstract] [Full Text] [Related]

  • 34. [The genetic study of retinoblastoma].
    Li AR, Fang QX, Luo CG, Xia RN, Zhou JM, Qiu JC, Li SJ, Hu SN, Wang H, Wang YP.
    Yan Ke Xue Bao; 1988 Jun; 4(2):73-7. PubMed ID: 3240815
    [No Abstract] [Full Text] [Related]

  • 35. Hereditary retinoblastoma: can balanced insertion entirely explain the differences of expressivity among families?
    Bonaïti-Pellié C, Clerget-Darpoux F, Babron MC.
    Hum Genet; 1990 Dec; 86(2):203-8. PubMed ID: 2265833
    [Abstract] [Full Text] [Related]

  • 36. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS, Kamel AA, El-Ruby M.
    Genet Couns; 2005 Dec; 16(4):393-402. PubMed ID: 16440882
    [Abstract] [Full Text] [Related]

  • 37. [Cytogenetic study of 257 mentally deficient patients in psychiatric hospitals].
    Bourgeois M, Bénézech M, Tournier-Zerbid N, Constant-Boy M, Benazet-Rissou J.
    Ann Med Psychol (Paris); 1975 Nov; 2(4):756-82. PubMed ID: 135524
    [Abstract] [Full Text] [Related]

  • 38. Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma.
    Amare Kadam PS, Ghule P, Jose J, Bamne M, Kurkure P, Banavali S, Sarin R, Advani S.
    Cancer Genet Cytogenet; 2004 Apr 01; 150(1):33-43. PubMed ID: 15041221
    [Abstract] [Full Text] [Related]

  • 39. [A case of bilateral retinoblastoma in light of genetic counseling].
    Broniarczyk-Lobowa A, Augustyniak E, Suprunowicz I, Debiec-Rychterowa M.
    Klin Oczna; 1985 Apr 01; 87(4):167-8. PubMed ID: 4046476
    [No Abstract] [Full Text] [Related]

  • 40. A case with 47,XXY,del(11)(q23) karotype-coexistence of Jacobsen and Klinefelter syndromes.
    Matheisel A, Babinska M, Wierzba J, Wozniak A, Nedoszytko B, Balcerska A, Limon J.
    Genet Couns; 2000 Apr 01; 11(3):267-71. PubMed ID: 11043435
    [Abstract] [Full Text] [Related]

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