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Localization of the spherocytosis gene to chromosome segment 8p11.22----8p21
1Department of Clinical Genetics, Kanazawa Medical University, Ishikawa, Japan.
Human Genetics
|January 1, 1988
Abstract:
A case of hereditary spherocytosis (HS) is reported. Cytogenetic study revealed a de novo minute deletion of chromosome 8. The critical portion which affected the expression of the HS phenotype appeared to be localized to 8p11.22----8p21.1.