Diagnosis of homozygous alpha-thalassemia in cultured amniotic-fluid fibroblasts. - Suppr | 超能文献

Diagnosis of homozygous alpha-thalassemia in cultured amniotic-fluid fibroblasts.

作者信息

Wong V, Ma H K, Todd D, Golbus M S, Dozy A M, Kan Y W

出版信息

N Engl J Med. 1978 Mar 23;298(12):669-70. doi: 10.1056/NEJM197803232981206.

DOI:10.1056/NEJM197803232981206

Abstract

摘要

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Diagnosis of homozygous alpha-thalassemia in cultured amniotic-fluid fibroblasts.

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Prenatal diagnosis of homozygous alpha thalassaemia by direct DNA analysis of uncultured amniotic fluid cells.通过对未培养羊水细胞进行直接DNA分析对纯合子α地中海贫血进行产前诊断。

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引用本文的文献

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Pathology-epitomes of progress: amniocentesis.病理学——进展缩影：羊膜穿刺术

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Human neutral alpha-glucosidase C: genetic polymorphism including a "null" allele.人中性α-葡萄糖苷酶C：包括“无效”等位基因在内的基因多态性。

Am J Hum Genet. 1980 Jul;32(4):497-507.

3

Prenatal diagnosis of homozygous alpha thalassaemia by direct DNA analysis of uncultured amniotic fluid cells.通过对未培养羊水细胞进行直接DNA分析对纯合子α地中海贫血进行产前诊断。

Br Med J (Clin Res Ed). 1984 May 5;288(6427):1327-9. doi: 10.1136/bmj.288.6427.1327.