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Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome 期刊论文
2019, 卷号: 18, 期号: 2, 页码: 261-265
作者:  Baig, Shahid Mahmood;  Fatima, Ambrin;  Tariq, Muhammad;  Khan, Tahir Naeem;  Ali, Zafar
收藏  |  浏览/下载:30/0  |  提交时间:2020/01/03


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