Retinoblastoma in a boy with a de novo mutation of a 13/18 translocation: The assumption that the retinoblastoma locus is at 13q141, particularly at the distal portion of it

No abstract is available for this paper.

• Publication year

  2004

• Venue

  Human Genetics

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/BF00569711PMID 6985466
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  1981cited by this paper
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  1981cited by this paper
• Further observations on a 13qXp translocation associated with retinoblastoma.

  1980cited by this paper
• Chromosomes in retinoblastoma patients

  1979cited by this paper
• Accumulation of Early Mitotic Cells in Ethidium Bromide-Treated Human Lymphocyte Cultures

  1979cited by this paper
• Trisomy for the distal end of the short arm of chromosome 3: a syndrome.

  1978cited by this paper
• Retinoblastoma and subband deletion of chromosome 13.

  1978cited by this paper
• Retinoblastoma in a patient with a 13qXp translocation.

  1977cited by this paper
• Partial deletions and trisomies of chromosome 13; Mapping of bands associated with particular malformations

  1976cited by this paper

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  2004cites this paper
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  2004cites this paper
• Is the interstitial delection of 13q in retinoblastoma patients not transmissible?

  2004cites this paper
• Advances in the analysis of chromosome alterations in human lung carcinomas.

  1997cites this paper
• The genetics of retinoblastoma, revisited.

  1994cites this paper
• Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.

  1994cites this paper
• A constitutional mutation within the retinoblastoma gene detected by PFGE

  1994cites this paper
• Cytogenetic and molecular investigation of a balanced Xq13q translocation in a patient with retinoblastoma.

  1992cites this paper
• Chromosome alterations in human small cell lung cancer: frequent involvement of 5q.

  1992cites this paper
• Chromosome alterations in 21 non‐small cell lung carcinomas

  1990cites this paper
• Report of the committee on clinical disorders and chromosomal deletion syndromes.

  1990cites this paper
• Report of the committee on clinical disorders and chromosomal deletion syndromes.

  1989cites this paper
• Constitutional karyotype in retinoblastoma. Case report and review of literature.

  1989cites this paper
• A case of Alagille's syndrome with translocation (4;14) (q21;q21).

  1989cites this paper
• Molecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptibility locus

  1989cites this paper
• Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients

  1988cites this paper
• Constitutional karyotypes in retinoblastoma.

  1987cites this paper
• Fragile sites, chromosome evolution, and human neoplasia

  1987cites this paper
• Structural evidence for the authenticity of the human retinoblastoma gene.

  1987cites this paper
• Partial monosomy 12p13.1----13.3.

  1987cites this paper
• Report of the committee on the genetic constitution of chromosomes 13, 14, 15 amd 16.

  1987cites this paper
• Translocation X;13 in a patient with retinoblastoma.

  1987cites this paper
• Evidence for the close linkage between lymphocyte cytosol polypeptide with molecular weight of 64,000 (LCP1) and esterase D.

  1985cites this paper
• The genetics of retinoblastoma.

  1985cites this paper
• Cytogenetic forms of retinoblastoma: their incidence in a survey of 66 patients.

  1985cites this paper
• Report of the Committee on the Genetic Constitution of Chromosomes 13, 14, 15 and 16.

  1985cites this paper
• Chromosome features of two retinoblastomas.

  1984cites this paper
• [Genetics and cancer].

  1984cites this paper
• Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus.

  1984cites this paper
• Report of the Committee on the Genetic Constitution of Chromosomes 13, 14, 15, 16 and 17.

  1984cites this paper
• Dominant susceptibility to cancer in man.

  1984cites this paper
• Bilateral retinoblastoma with de novo constitutional balanced translocation t(2;9)(q11;q11)

  1984cites this paper
• The chromosomal basis of human neoplasia.

  1983cites this paper
• High-resolution cytogenetics.

  1983cites this paper
• Retinoblastoma: A model for the study of carcinogenesis in humans

  1983cites this paper