Kitatani M, Chiyo H, Ozaki M, Shike S, Miwa S
Department of Clinical Genetics, Kanazawa Medical University, Ishikawa, Japan.
Hum Genet. 1988 Jan;78(1):94-5. doi: 10.1007/BF00291244.
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.
报告了一例遗传性球形红细胞增多症(HS)。细胞遗传学研究发现8号染色体有一个新生的微小缺失。影响HS表型表达的关键部分似乎定位于8p11.22----8p21.1。