Partial monosomy 12p13.1----13.3.

Author:

Romain D R,Goldsmith J,Columbano-Green L M,Chapman C J,Smythe R H,Parfitt R G

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference15 articles.

1. The Costendader memorial lecturc: genesis and genetics of retinoblastoma;Francois, J.;J Pediatr Ophthalmol Strabismus,1979

2. Retinoblastoma: host resistance and 13qchromosome deletion;Matsunaga, E.;Hum Genet,1980

3. 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;Motegi, T.; Komatsu, M.; Nakazato, Y.;Hum Genet,1982

4. Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus;Ward, P.; Packman, S.; Loughman, W.;J Med Genet; Possible inactivation of part of chromosome 13 duc to 13qXp translocation associated with retinoblastoma,1984

5. Genetic evidence for the inactivation of a human autosomal locus attached to an inactive X chromosome;Mohandas, T.; Sparkes, R.S.; Shapiro, L.J.;Am J Hum Genet,1982

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