Second-Trimester Detection of Mowat-Wilson Syndrome Using Comparative Genomic Hybridization Microarray Testing
Publication in refereed journal


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摘要BACKGROUND: Fetuses with increased nuchal translucency but apparently normal karyotypes may have small genetic defects that are undetectable by conventional cytogenetic studies. Microarray comparative genomic hybridization (array comparative genomic hybridization) may help prenatal diagnosis by revealing small genetic defects.
著者Choy KW, To KF, Chan AWH, Lau TK, Leung TY
期刊名稱Obstetrics and Gynecology
出版年份2010
月份2
日期1
卷號115
期次2
出版社Lippincott, Williams & Wilkins: No Hybrid Open Access
頁次462 - 465
國際標準期刊號0029-7844
電子國際標準期刊號1873-233X
語言英式英語
Web of Science 學科類別Obstetrics & Gynecology; OBSTETRICS & GYNECOLOGY

上次更新時間 2021-25-02 於 00:58