Neurofibromatosis type 1.

E. Legius, M. Descheemaeker, J. Fryns, H. van den Berghe
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引用次数: 2
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1型神经纤维瘤病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genetic Counseling
Genetic Counseling 医学-生物工程与应用微生物
CiteScore
0.14
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Every day researchers are learning more about the genetics of common diseases and how those diseases run in families. If you have an inherited disease in your family, a genetic counseling session can help you understand your personal risk or the risk for other family members. It can also help you learn what testing, surveillance, prevention strategies, or research trials may be right for your situation. In most cases, a genetic counselor will lead the session, but some nurses, doctors, and medical geneticists are also trained to do genetic counseling.
期刊最新文献
Preconception care. Familial cylindromatosis. Attention deficit, impulsivity characteristics and visual perception in biological parents of attention deficit and normal control children Neurofibromatosis Type 1 Neurofibromatosis type 1.
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