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Journal Abstract Search

152 related items for PubMed ID: 7953248

  • 21. Cytogenetic analysis of retinoblastoma: evidence for multifocal origin and in vivo gene amplification.
    Chaum E, Ellsworth RM, Abramson DH, Haik BG, Kitchin FD, Chaganti RS.
    Cytogenet Cell Genet; 1984; 38(2):82-91. PubMed ID: 6467991
    [Abstract] [Full Text] [Related]

  • 22. Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosis.
    Junien C, Despoisse S, Turleau C, Nicolas H, Picard F, Le Marec B, Kaplan JC, de Grouchy J.
    Cancer Genet Cytogenet; 1982 Aug; 6(4):281-7. PubMed ID: 7116321
    [Abstract] [Full Text] [Related]

  • 23. A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q.
    Motegi T, Kaga M, Yanagawa Y, Kadowaki H, Watanabe K, Inoue A, Komatsu M, Minoda K.
    Hum Genet; 1983 Aug; 64(2):160-2. PubMed ID: 6885051
    [Abstract] [Full Text] [Related]

  • 24. The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions.
    Cowell JK, Thompson E, Rutland P.
    Arch Dis Child; 1987 Jan; 62(1):8-11. PubMed ID: 3813643
    [Abstract] [Full Text] [Related]

  • 25. Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients.
    Ejima Y, Sasaki MS, Kaneko A, Tanooka H.
    Hum Genet; 1988 Jun; 79(2):118-23. PubMed ID: 3391612
    [Abstract] [Full Text] [Related]

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

  • 27. The genetics of retinoblastoma.
    Stahl A, Levy N, Wadzynska T, Sussan JM, Jourdan-Fonta D, Saracco JB.
    Ann Genet; 1994 Jun; 37(4):172-8. PubMed ID: 7710251
    [Abstract] [Full Text] [Related]

  • 28. Genetics of retinoblastoma: a study.
    Mateu E, Sánchez F, Nájera C, Beneyto M, Castell V, Hernández M, Serra I, Prieto F.
    Cancer Genet Cytogenet; 1997 May; 95(1):40-50. PubMed ID: 9140452
    [Abstract] [Full Text] [Related]

  • 29. Interstitial deletion of 13q associated with polymicrogyria.
    Kogan JM, Egelhoff JC, Saal HM.
    Am J Med Genet A; 2008 Apr 01; 146A(7):910-6. PubMed ID: 18324687
    [Abstract] [Full Text] [Related]

  • 30. Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locus.
    Horsthemke B, Barnert HJ, Greger V, Passarge E, Höpping W.
    Lancet; 1987 Feb 28; 1(8531):511-2. PubMed ID: 2881072
    [No Abstract] [Full Text] [Related]

  • 31. Interstitial deletion of chromosome 13 involving the region 13q14.
    Pankau R, Johannson W, Grote W, Dörner K, Tolksdorf M.
    Hum Genet; 1987 Nov 28; 77(3):292-3. PubMed ID: 3679214
    [Abstract] [Full Text] [Related]

  • 32. [Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients].
    Munier F, Balmer A, von Moos C, Pescia G, Gailloud C, van Melle G, Thonney F, Gaide AC, Allaz MJ, Rutz HP.
    Klin Monbl Augenheilkd; 1991 May 28; 198(5):419-24. PubMed ID: 1886375
    [Abstract] [Full Text] [Related]

  • 33. Retinoblastoma: host resistance and 13q- chromosomal deletion.
    Matsunaga E.
    Hum Genet; 1980 May 28; 56(1):53-8. PubMed ID: 7203480
    [Abstract] [Full Text] [Related]

  • 34. Chromosomal abnormalities in human retinoblastoma. A review.
    Potluri VR, Helson L, Ellsworth RM, Reid T, Gilbert F.
    Cancer; 1986 Aug 01; 58(3):663-71. PubMed ID: 3524791
    [Abstract] [Full Text] [Related]

  • 35. The importance of excluding 13q deletion mosaicism in the diagnosis of retinoblastoma associated with dysmorphic features.
    Van Esch H, Aerssens P, Fryns JP.
    Genet Couns; 2005 Aug 01; 16(1):91-3. PubMed ID: 15844785
    [No Abstract] [Full Text] [Related]

  • 36. A deleted chromosome no. 13 in human retinoblastoma cells: relevance to tumorigenesis.
    Balaban-Malenbaum G, Gilbert F, Nichols WW, Hill R, Shields J, Meadows AT.
    Cancer Genet Cytogenet; 1981 Apr 01; 3(3):243-50. PubMed ID: 7284985
    [Abstract] [Full Text] [Related]

  • 37. 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 01; 48(2):265-9. PubMed ID: 2397457
    [Abstract] [Full Text] [Related]

  • 38. Retinoblastoma and retinoma occurring in a child with a translocation and deletion of the long arm of chromosome 13.
    Keith CG, Webb GC.
    Arch Ophthalmol; 1985 Jul 01; 103(7):941-4. PubMed ID: 4015485
    [Abstract] [Full Text] [Related]

  • 39. Genetic and cytogenetic analysis of patients showing reduced esterase-D levels and mental retardation from a survey of 500 individuals with retinoblastoma.
    Cowell JK, Hungerford J, Rutland P, Jay M.
    Ophthalmic Paediatr Genet; 1989 Jun 01; 10(2):117-27. PubMed ID: 2779982
    [Abstract] [Full Text] [Related]

  • 40. [Genetics of retinoblastoma].
    Minoda K.
    Nihon Rinsho; 1995 Nov 01; 53(11):2774-8. PubMed ID: 8538043
    [Abstract] [Full Text] [Related]

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