Hereditary retinoblastoma: can balanced insertion entirely explain the differences of expressivity among families?

[1]  K. Tan,et al.  Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene. , 1989, American journal of human genetics.

[2]  S. Hinrichs,et al.  Structural evidence for the authenticity of the human retinoblastoma gene. , 1987, Science.

[3]  W. Lee,et al.  Human retinoblastoma susceptibility gene: cloning, identification, and sequence , 1987, Science.

[4]  Stephen H. Friend,et al.  A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma , 1986, Nature.

[5]  Raymond L. White,et al.  Homozygosity of chromosome 13 in retinoblastoma. , 1984, The New England journal of medicine.

[6]  T. P. Dryja,et al.  Expression of recessive alleles by chromosomal mechanisms in retinoblastoma , 1983, Nature.

[7]  B. Gallie,et al.  Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma , 1983, Nature.

[8]  W. Benedict,et al.  Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D. , 1983, Science.

[9]  L. Strong,et al.  Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation. , 1981, Science.

[10]  E. Matsunaga Retinoblastoma: Host resistance and 13q- chromosomal deletion , 1980, Human Genetics.

[11]  F. Demenais,et al.  Diseases having two classes of severity: estimation of the proportions of each manifestation by maximum likelihood. , 1980, Biometrics.

[12]  C. Bonaïti‐pellié,et al.  Excess of cancer deaths in grandparents of patients with retinoblastoma. , 1980, Journal of medical genetics.

[13]  U. Francke,et al.  Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas , 1979, Clinical genetics.

[14]  E. Matsunaga Hereditary retinoblastoma: delayed mutation or host resistance? , 1978, American journal of human genetics.

[15]  E. Matsunaga Hereditary retinoblastoma: Penetrance, expressivity and age of onset , 1976, Human Genetics.

[16]  J. Feingold,et al.  Étude génétique du rétinoblastome , 1974, Humangenetik.

[17]  A. Sorsby Bilateral Retinoblastoma: A Dominantly Inherited Affection , 1972, British medical journal.

[18]  A. Knudson Mutation and cancer: statistical study of retinoblastoma. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[19]  M. Macklin A study of retinoblastoma in Ohio. , 1960, American journal of human genetics.

[20]  D. Cogan,et al.  Frequency of genetic transmission of sporadic retinoblastoma. , 1957, A.M.A. archives of ophthalmology.

[21]  By CHARLOTTE Auerbach A POSSIBLE CASE OF DELAYED MUTATION IN MAN , 1956, Annals of human genetics.

[22]  J. Neel,et al.  Genetics of retinoblastoma. , 1951, A.M.A. archives of ophthalmology.

[23]  C. Bonaïti‐pellié,et al.  Segregation analysis in hereditary retinoblastoma , 2004, Human Genetics.

[24]  C. Junien,et al.  Retinoblastoma-del(13q14): Report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D , 2004, Human Genetics.

[25]  A. Knudson Model hereditary cancers of man. , 1983, Progress in nucleic acid research and molecular biology.

[26]  A. Leblanc,et al.  Two cases of del(13q)-retinoblastoma and two cases of partial trisomy due to a familial insertion. , 1983, Annales de genetique.

[27]  J. Herrmann Delayed mutation as a cause of retinoblastoma: application to genetic counseling. , 1976, Birth defects original article series.

[28]  E. Matsunaga,et al.  Retinoblastoma in Japan--Follow-up survey of spordic cases , 1976 .

[29]  R. Ellsworth The practical management of retinoblastoma. , 1969, Transactions of the American Ophthalmological Society.

[30]  J. Schappert-Kimmijser,et al.  The heredity of retinoblastoma. , 1966, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.