Proximal 15q monosomy.
作者信息
Duckett D P
出版信息
J Med Genet. 1982 Oct;19(5):393-4. doi: 10.1136/jmg.19.5.393-a.
Abstract
摘要
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Proximal 15q monosomy.近端15号染色体长臂单体性
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引用本文的文献
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Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.普拉德-威利综合征病例中的不平衡相互易位
Hum Genet. 1984;67(2):156-61. doi: 10.1007/BF00272991.
本文引用的文献
1
Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.相互易位：一种通过粗线期图绘制预测不平衡分离模式的方法。
Hum Genet. 1980;55(2):209-22. doi: 10.1007/BF00291769.
2
Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.15号染色体缺失是普拉德-威利综合征的病因。
N Engl J Med. 1981 Feb 5;304(6):325-9. doi: 10.1056/NEJM198102053040604.
3
Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.15号染色体异常与普拉德-威利综合征：40例随访报告
Am J Hum Genet. 1982 Mar;34(2):278-85.
4
Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.相邻2减数分裂分离。1例由家族性13号染色体长臂；15号染色体长臂平衡易位导致的病例报告及文献复习
Hum Genet. 1981;58(4):377-86. doi: 10.1007/BF00282819.
5
Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.人类中的相互易位。3:1减数分裂分离导致产生47条或45条染色体的后代。
J Med Genet. 1975 Mar;12(1):29-43. doi: 10.1136/jmg.12.1.29.
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