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发表于 2025-3-21 18:43:36
书目名称Studies in Inherited Metabolic Disease影响因子(影响力)<br> http://impactfactor.cn/if/?ISSN=BK0880858<br><br> <br><br>书目名称Studies in Inherited Metabolic Disease影响因子(影响力)学科排名<br> http://impactfactor.cn/ifr/?ISSN=BK0880858<br><br> <br><br>书目名称Studies in Inherited Metabolic Disease网络公开度<br> http://impactfactor.cn/at/?ISSN=BK0880858<br><br> <br><br>书目名称Studies in Inherited Metabolic Disease网络公开度学科排名<br> http://impactfactor.cn/atr/?ISSN=BK0880858<br><br> <br><br>书目名称Studies in Inherited Metabolic Disease被引频次<br> http://impactfactor.cn/tc/?ISSN=BK0880858<br><br> <br><br>书目名称Studies in Inherited Metabolic Disease被引频次学科排名<br> http://impactfactor.cn/tcr/?ISSN=BK0880858<br><br> <br><br>书目名称Studies in Inherited Metabolic Disease年度引用<br> http://impactfactor.cn/ii/?ISSN=BK0880858<br><br> <br><br>书目名称Studies in Inherited Metabolic Disease年度引用学科排名<br> http://impactfactor.cn/iir/?ISSN=BK0880858<br><br> <br><br>书目名称Studies in Inherited Metabolic Disease读者反馈<br> http://impactfactor.cn/5y/?ISSN=BK0880858<br><br> <br><br>书目名称Studies in Inherited Metabolic Disease读者反馈学科排名<br> http://impactfactor.cn/5yr/?ISSN=BK0880858<br><br> <br><br>
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发表于 2025-3-21 21:10:33
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Affirm
发表于 2025-3-22 02:01:11
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Generic-Drug
发表于 2025-3-22 07:22:34
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diskitis
发表于 2025-3-22 10:11:56
Prenatal Diagnosis of Disorders of Galactose Metabolismvillus biopsies and by galactitol estimation in amniotic fluid supernatant. Although the long-term outcome of patients treated on a galactose-restricted diet is recognized to be unsatisfactory, prenatal diagnosis is only rarely performed with a view to terminating the affected pregnancy.
MOT
发表于 2025-3-22 16:15:12
Prefacesampling methods and genetic in relation to techniques for analysis. Against this background, the aim of the Symposium was to provide an overview of the current status of prenatal and perinatal diagnosis of inborn errors of metabolism.
Hyperlipidemia
发表于 2025-3-22 19:34:09
The Salience of Garrod’s ‘Molecular Groupings’ and ‘Inborn Factors in Disease’nzymes are normally homopolymeric; (3) in clinical severity of ‘monogenic’ disease (e.g. familial hypercholesterolaemia and muscular dystrophy) when variation is not explained by allelic heterogeneity. The associated chemical individuality in each case can be used to identify risk and thus as a mode of predictive medicine.
娴熟
发表于 2025-3-23 01:16:21
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轻率的你
发表于 2025-3-23 03:04:30
A Clinician’s View of the Mass Screening of the Newborn for Inherited Diseases: Current Practice and. A simple tool for early detection is now available and the population afflicted with a mutant gene which causes major health problems should receive special attention from its government. It is too early to offer any comment about cystic fibrosis screening; further developments must be awaited.
Conquest
发表于 2025-3-23 06:41:19
A Clinical Biochemist’s View of the Investigation of Suspected Inherited Metabolic Diseasevidual patient. A full metabolic laboratory investigation programme is described and illustrated with some examples of abnormal metabolite patterns. Diagnostic results over a 2-year period are presented.