The need for care in the use of linkage analysis for genetic diagnosis in small families, with particular reference to uniparental disomy.
作者信息
Woods C G, Edwards J H
出版信息
Am J Hum Genet. 1992 Nov;51(5):1171-2.
Abstract
摘要
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本文引用的文献
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Uniparental disomy as a mechanism for human genetic disease.单亲二体作为人类遗传疾病的一种机制。
Am J Hum Genet. 1988 Feb;42(2):217-26.
2
Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?一名囊性纤维化患者的7号染色体等臂双体：单亲二体在人类中会很常见吗？
Am J Hum Genet. 1989 Sep;45(3):373-80.
3
Non-paternity and prenatal genetic screening.非父系关系与产前基因筛查
Lancet. 1991 Nov 2;338(8775):1151. doi: 10.1016/0140-6736(91)92013-r.
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