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8个假肥大型肌营养不良症家系产前基因诊断 被引量:3

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出处 《中华检验医学杂志》 CAS CSCD 北大核心 2003年第1期52-53,共2页 Chinese Journal of Laboratory Medicine
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  • 1黄尚志,中华医学遗传学杂志,1995年,12卷,179页

共引文献5

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  • 1黄文,张成,谢有梅,陈松林,张为西,卢锡林,姚晓黎,曾缨.应用多个微卫星DNA位点进行Duchenne/Becker肌营养不良症携带者的检测[J].中华医学遗传学杂志,2004,21(3):224-228. 被引量:12
  • 2高文英,佟彤,陈悦,卜桦,张玉琴.应用PCR-STR方法对DMD高危家族产前基因诊断[J].中国优生与遗传杂志,2006,14(2):13-14. 被引量:2
  • 3Chamberlain JS,Gibbs RA,Ranier JE. Deletion Screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification[J].Nucleic Acids Research,1988.11141-11156.
  • 4Beggs AH,Koenig M,Boyce FM. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction[J].Human Genetics,1990.45.
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  • 6Mehler MF. Brain dystrophin,neurogenetics and mental retardation[J].Brain Research Reviews,2000.277-307.
  • 7Hammed SA,Sutherland-Smith AJ,Gorospe JRM. DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy[J].Clinical Genetics,2005.68-79.
  • 8Madhuri RH,Ephrem LH,Chin JG. Microarray-based mutation detection in the dystrophin gene[J].Human Mutation,2008.1091-1099.
  • 9Alcántara Ortigoza MA,Aguinaga Ríos M,González del Angel A. Prenatal molecular diagnosis of a DMD carrier female fetus by chorionic villus sampling and linkage analysis.A case report and literature review[J].Ginecologia Y Obstetricia De Mexico,2009.103-109.
  • 10Lai KK,Lo IF,Tong TM. Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification(MLPA)[J].Clinical Biochemistry,2006.367-372.

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