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发表于 2025-3-21 16:13:44
书目名称Genetic Counseling for Adult Neurogenetic Disease影响因子(影响力)<br> http://figure.impactfactor.cn/if/?ISSN=BK0382471<br><br> <br><br>书目名称Genetic Counseling for Adult Neurogenetic Disease影响因子(影响力)学科排名<br> http://figure.impactfactor.cn/ifr/?ISSN=BK0382471<br><br> <br><br>书目名称Genetic Counseling for Adult Neurogenetic Disease网络公开度<br> http://figure.impactfactor.cn/at/?ISSN=BK0382471<br><br> <br><br>书目名称Genetic Counseling for Adult Neurogenetic Disease网络公开度学科排名<br> http://figure.impactfactor.cn/atr/?ISSN=BK0382471<br><br> <br><br>书目名称Genetic Counseling for Adult Neurogenetic Disease被引频次<br> http://figure.impactfactor.cn/tc/?ISSN=BK0382471<br><br> <br><br>书目名称Genetic Counseling for Adult Neurogenetic Disease被引频次学科排名<br> http://figure.impactfactor.cn/tcr/?ISSN=BK0382471<br><br> <br><br>书目名称Genetic Counseling for Adult Neurogenetic Disease年度引用<br> http://figure.impactfactor.cn/ii/?ISSN=BK0382471<br><br> <br><br>书目名称Genetic Counseling for Adult Neurogenetic Disease年度引用学科排名<br> http://figure.impactfactor.cn/iir/?ISSN=BK0382471<br><br> <br><br>书目名称Genetic Counseling for Adult Neurogenetic Disease读者反馈<br> http://figure.impactfactor.cn/5y/?ISSN=BK0382471<br><br> <br><br>书目名称Genetic Counseling for Adult Neurogenetic Disease读者反馈学科排名<br> http://figure.impactfactor.cn/5yr/?ISSN=BK0382471<br><br> <br><br>
incisive
发表于 2025-3-21 20:42:32
DFT - Diskrete Fourier-Transformationatomy, pathology, etiology, and genetics, none of which are perfect. Classification by genetic etiology is complicated by heterogeneity, in which many genes cause the same phenotype, as well as pleiotropy, in which mutations in a single gene can result in different phenotypes. Genetic counseling for
FLAX
发表于 2025-3-22 00:33:38
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exceed
发表于 2025-3-22 05:32:14
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Inkling
发表于 2025-3-22 10:26:02
The Loss of the Sleipner Condeep Platformor inherited. Classifications are made by age of onset, affected body part, whether it is primary, secondary or heredodegenerative, and by the presence or absence of other movement disorders. Numerous genes can cause dystonia, complicating testing and diagnosis. Inheritance patterns can be autosomal
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发表于 2025-3-22 13:10:44
System of Organizing and Building DIISria, and, often, abnormal oculomotor control. Age of onset of these disorders ranges from infancy to late life, and may include many additional clinical features such as neuropathy, cognitive dysfunction, and parkinsonism. Genetic counseling is frequently complicated by the overlap in phenotypes, an
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发表于 2025-3-22 18:01:35
Substanzmissbrauch und Substanzabhängigkeitmon causes of dementia is Alzheimer’s disease. Dementia may have associated motor symptoms that can develop before or after the cognitive dysfunction. This section reviews many of the genetic counseling issues, including complexity of family history with both sporadic and inherited forms of dementia
人类学家
发表于 2025-3-23 00:32:05
Jürgen Margraf,Silvia Schneider, and .. Susceptibility genes such as APOE contribute to risk in a far larger number of cases. Predictive testing is available for the autosomal dominant genes, but is not recommended for risk genes as they are neither necessary nor sufficient to cause AD. Genetic testing is complicated by capacity
GROSS
发表于 2025-3-23 02:42:58
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团结
发表于 2025-3-23 08:10:12
https://doi.org/10.1007/978-3-642-84501-7a (FFI). Ten to fifteen percent of prion disease has a genetic etiology. Inherited forms of all 3 diseases are due to mutations in the . gene. The phenotype conferred by a specific mutation can be further modified by a polymorphism at codon 29. Additionally age of onset and symptom presentation cann