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Conclusion: Routine glucose testing is indicated in large-for-gestational-age newborn infants of nondiabetic mothers.
Genetics professionals can also help those who have limited or no family history information, such as those who are adopted, those who were donor-conceived, or those not in touch with close relatives, determine what other disease risk factors may be present and whether genetic testing is indicated in the absence of a detailed family history.
Our findings also suggest that such testing is indicated, in the right setting, even when imaging reveals a structural abnormality that might be considered the cause.
Electrophysiological testing is indicated in the investigation of syncope in younger adults with an abnormal ECG and preexisting heart disease, indicating a cardiac cause (ESC 2004).
A1C testing is indicated in children in whom diabetes is suspected but the classic symptoms and a casual plasma glucose >200 mg/dl (>11.1 mmol/l) are not found.
There is general agreement that predictive genetic testing is indicated in asymptomatic relatives of a patient with HCM when a definitive disease-causing mutation has been previously characterized in the family.
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For each experiment, the corresponding statistics test is indicated in the figure legend.
CusA concentration in the different detergents tested is indicated in table 1.
The applied test is indicated in each figure legend.
For each test, the number of mice (N) tested is indicated in the respective figure caption.
The number of patients tested is indicated in each box (n).
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