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https://doi.org/10.1007/bf00291244
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Cite Journal: Human Genetics |  Publication Date: Jan 1, 1988 |
 Citations: 38 |
Affiliation: Kanazawa Medical University, The University of Tokyo
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.
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