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I WT1 TC

WT-1 tumor suppressor, technical only

WT-1 tumor suppressor, by IHC, technical only
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IHC
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I WT1

WT-1 tumor suppressor

WT-1 tumor suppressor, by IHC
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IHC
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WARF*

Warfarin Sensitivity Testing

CYP2C9 and VKORC1 allele, Cytochrome P450 ,Coumadin
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Molecular
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F WIL

Williams Syndrome deletion 7q11.2*

Williams syndrome is a rare genetic disorder found in approximately 1 in 7,500-20,000 people. A deletion on chromosome 7 is the cause for the disorder. This region includes several genes…
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FISH
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F WH

Wolf-Hirschhorn Syndrome deletion 4p16.3*

Wolf-Hirschhorn syndrome, causing deletion of the short arm of chromosome 4, affects approximately 1 in 50,000 births.
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FISH
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