Prenatal and postnatal prevalence of Turner's syndrome. Data presented were insufficient to challenge specificity of prenatal diagnosis.
作者信息
van der Sijs-Bos C J, Stigter R H, Christiaens G C, Leschot J
出版信息
BMJ. 1996 Jul 6;313(7048):47-8. doi: 10.1136/bmj.313.7048.47b.
Abstract
摘要
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Prenatal and postnatal prevalence of Turner's syndrome. Data presented were insufficient to challenge specificity of prenatal diagnosis.特纳综合征的产前和产后患病率。所呈现的数据不足以质疑产前诊断的特异性。
BMJ. 1996 Jul 6;313(7048):47-8. doi: 10.1136/bmj.313.7048.47b.
2
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Prenatal and postnatal prevalence of Turner's syndrome. No scientific evidence for study's conclusions.特纳综合征的产前和产后患病率。该研究结论缺乏科学依据。
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Risk of 45,X karyotype in offspring of Turner's syndrome patients.特纳综合征患者后代出现45,X核型的风险。
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[Prenatal Turner's syndrome].
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本文引用的文献
1
Prenatal and postnatal prevalence of Turner's syndrome: a registry study.特纳综合征的产前和产后患病率：一项登记研究。
BMJ. 1996 Jan 6;312(7022):16-21. doi: 10.1136/bmj.312.7022.16.
2
Monosomy X found at first trimester CVS: a diagnostic and counselling dilemma.孕早期绒毛取样检测发现X单体：诊断与咨询困境
Clin Genet. 1990 Mar;37(3):236-7. doi: 10.1111/j.1399-0004.1990.tb03510.x.
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