Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity

Author:

Connolly M. J.,Payne R. H.,Johnson G.,Gallie B. L.,Allderdice P. W.,Marshall W. H.,Lawton R. D.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference15 articles.

1. Bonaïti-Pellié C, Briard-Guillemot ML (1981) Segregation analysis in hereditary retinoblastoma. Hum Genet 57:411?419

2. Bundey S, Morten JEN (1981) An unusual pedigree with retinoblastoma. Does it shed light on the delayed mutation and host resistance theories? Hum Genet 59:434?436

3. Carlson EA, Desnick RJ (1979) Mutational mosaicism and genetic counselling in retinoblastoma. Am J Med Genet 4:365?381

4. Duane TB (1980) Clinical ophthalmology, vol 3. Harper and Row, Hagerstown, p 13

5. Gallie BL, Phillips RA (1982) Multiple manifestations of the retinoblastoma gene. In: Cotlier E, Maumenee I, Berman ER (eds) Genetic eye diseases: Retinitis pigmentosa and other inherited eye diseases. Birth Defects 18:689?701

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