Localization of the spherocytosis gene to chromosome segment 8p11.22----8p21
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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Veröffentlicht in: | Human genetics 1988-01, Vol.78 (1), p.94-95 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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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ISSN: | 0340-6717 |