Retina · 1994 · 106 citations · 34 references
Life SciencesGeneticsMolecular GeneticsCancer GeneticsHuman GeneticsMedical GeneticsGenetic DisordersGenetic LinkageGermline Cancer PredispositionHereditary Cancer SyndromesFamilial RetinoblastomaHereditary RetinoblastomaIncomplete PenetranceRetinoblastoma Family ProteinsRetinoid Receptors
In one family with low-penetrance retinoblastoma, a germ-line deletion is shared by affected and unaffected, obligate carriers. The deletion encompasses exon 4 of the retinoblastoma gene and corresponds to a mutant protein without residues 127-166. In a second family, RFLP analysis shows that two distant relatives have independently derived mutations. These families, together with others reported elsewhere, indicate that attributes of alleles at the retinoblastoma locus specify penetrance.
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A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
Stephen Friend, René Bernards, Snezna Rogelj et al. · Nature · 1986 · 3K citations · Full text
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
Webster K. Cavenee, Thaddeus P. Dryja, Robert A. Phillips et al. · Nature · 1983 · 1.9K citations