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Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22.
Genetic and comparative mapping of genes dysregulated in mouse hearts lacking the Hand2 transcription factor gene.
IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human disease.
Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiency.
A microsatellite-based multipoint index map of human chromosome 22.
Twelve new polymorphic microsatellites on human chromosome 22.
The gene encoding human TFE3, a transcription factor that binds the immunoglobulin heavy-chain enhancer, maps to Xp11.22.