Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity.
作者信息
Parker C E, Koch R, Mavalwala J, Derencsenyi A, Hatashita A
出版信息
Clin Pediatr (Phila). 1969 Aug;8(8):453-8. doi: 10.1177/000992286900800808.
PMID:5797429
Abstract
摘要
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Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity.与触珠蛋白或过氧化氢酶活性丧失无关的D1染色体短臂家族性缺失（46, XX, 13 p-）
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A child with a ring G chromosome (46,XX, Gr).一名患有环状G染色体的儿童（46,XX, Gr）。
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引用本文的文献
1
Short arm deletion of chromosome 14.14号染色体短臂缺失
Humangenetik. 1972;15(1):33-8. doi: 10.1007/BF00273429.
2
Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.群体细胞遗传学、常染色体基因位点的定位、核型与表型的相关性。人类细胞遗传学进展报告。
Humangenetik. 1970;9(1):1-15. doi: 10.1007/BF00696007.
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Familial short arm deletion of chromosome no. 15.家族性15号染色体短臂缺失
Humangenetik. 1974;21(3):283-6. doi: 10.1007/BF00279024.
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Frequency of deletion of short arm satellites in acrocentric chromosomes.近端着丝粒染色体短臂卫星序列缺失的频率
J Med Genet. 1974 Jun;11(2):177-80. doi: 10.1136/jmg.11.2.177.
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