Implications of diagnostic delay in Duchenne muscular dystrophy.
作者信息
O'Brien T, Sibert J R, Harper P S
出版信息
Br Med J (Clin Res Ed). 1983 Oct 15;287(6399):1106-7. doi: 10.1136/bmj.287.6399.1106.
Abstract
摘要
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本文引用的文献
1
The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy.利用连锁DNA多态性对杜氏肌营养不良症家系进行基因型预测。
J Med Genet. 1983 Aug;20(4):252-4. doi: 10.1136/jmg.20.4.252.
2
Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequences.利用两个克隆的DNA序列进行连锁研究显示杜氏肌营养不良不存在遗传异质性。
J Med Genet. 1983 Aug;20(4):249-51. doi: 10.1136/jmg.20.4.249.
3
Newborn screening for Duchenne muscular dystrophy.杜氏肌营养不良症的新生儿筛查
Pediatrics. 1975 Jan;55(1):30-4.
4
Controversies about Duchenne muscular dystrophy. (1) Neonatal screening.
Dev Med Child Neurol. 1979 Jun;21(3):390-3. doi: 10.1111/j.1469-8749.1979.tb01633.x.
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