Property:AnswerB

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Showing 20 pages using this property.
W
WBR0085 +
Infant serum – VDRL  +
WBR0086 +
''Listeria monocytogenes''  +
WBR0087 +
Locus heterogeneity  +
WBR0088 +
CD4 receptors  +
WBR0089 +
Epinephrine  +
WBR0090 +
Increase in FEV1 of 15% after giving inhaled albuterol  +
WBR0092 +
Norepinephrine reuptake inhibitor  +
WBR0093 +
Serotonin and norepinephrine reuptake inhibitor  +
WBR0094 +
Norepinephrine reuptake inhibitor  +
WBR0095 +
''STK11'' gene  +
WBR0096 +
The disease is associated with subcutaneous deposits  +
WBR0097 +
Mutation of three copies of the alpha globin gene  +
WBR0098 +
Expansion of CAA repeats  +
WBR0099 +
5'...GGT ACG TGA AGA AGA TCT...3'  +
WBR0100 +
Gene deletion  +
WBR0101 +
Ataxia  +
WBR0102 +
The patient's condition is caused by defects in hydroxylation of proline residues  +
WBR0103 +
The patient’s condition is caused by inactivating mutations in the ''FGFR3'' gene; and his children have a 50% chance of developing dwarfism.  +
WBR0104 +
Caused by a defect of cilium flow response  +
WBR0105 +
Mutation of ''TGFBR2''  +
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