荧光原位杂交法分析先天性卵巢发育不全综合征患者标记染色体
被引量:3
出处
《中华检验医学杂志》
CAS
CSCD
北大核心
2005年第10期1053-1054,共2页
Chinese Journal of Laboratory Medicine
基金
国家"十五"科技攻关资助项目(2004BA720A04)
参考文献2
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同被引文献13
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1梁雁,罗小平.Turner综合征患儿标记染色体的来源研究[J].中华医学遗传学杂志,2005,22(4):435-437. 被引量:14
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10胡晓峰,朱宝生,虎宝先,林汉华,舒丹,李春华,刘希贤.应用FISH和PCR技术鉴别Turner综合征患者标记染色体起源[J].中华医学遗传学杂志,1999,16(6):392-394. 被引量:1
引证文献3
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3徐红艳,张东光,熊枫,黄慧,杨文萍,吴艳.荧光原位杂交技术在儿童Turner综合征中的应用研究[J].江西医药,2021,56(2):260-262. 被引量:1
二级引证文献15
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2孟金来,贾颐舫,王谢桐.染色体微阵列分析技术在产前遗传性疾病诊断中的应用进展[J].现代妇产科进展,2015,24(5):390-393. 被引量:13
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3李素萍,金玉霞,刘晓丹,宋勤浩,朱斌臻,周赤燕,沈华祥,苗正友.核型分析结合单核苷酸多态性微阵列技术在一父源性染色体平衡易位家系中的应用[J].中国优生与遗传杂志,2016,24(3):26-29. 被引量:1
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4曾艳,范佳鸣,许平,张丽芳,钱飞燕,罗婷婷.两例微小额外标记染色体的产前诊断[J].中华医学遗传学杂志,2016,33(4):498-500. 被引量:1
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5薛江,李桂梅.先天性卵巢发育不全综合征研究进展[J].山东医药,2003,43(24):61-62. 被引量:1
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