Property:AnswerD
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1098
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Showing 20 pages using this property.
W
WBR0084
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Deer fly
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WBR0085
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Infant serum – FTA-ABS
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WBR0086
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''Trichomonas spp.''
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WBR0087
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Anticipation
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WBR0088
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CCR5 receptors
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WBR0089
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ADH
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WBR0090
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A peak expiratory flow measurement 30% below the predicted normal value for the patient
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WBR0092
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Alpha-2 receptor antagonist
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WBR0093
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Alpha-2 receptor antagonist
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WBR0094
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Alpha-2 receptor antagonist
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WBR0095
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''WNT'' gene
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WBR0096
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The disease is associated with increased chylomicrons
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WBR0097
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Mutation of spectrin
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WBR0098
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Expansion of CGG repeats
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WBR0099
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5'...GGC TAC GTG ATG AAG TCT...3'
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WBR0100
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Gene duplication
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WBR0101
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Eczema
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WBR0102
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The patient's condition is associated with nephritis
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WBR0103
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The patient’s condition is caused by activating mutations in the ''FGFR3'' gene; and his children have a near 25% chance of developing dwarfism.
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WBR0104
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Caused by a mutant gene located on chromosome 18
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