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Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center

Disorder	Genes	Test Method	Lab Info	Product code
Achromatopsia 2 - Sequence analysis of the entire coding region	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	Achromatopsia 2				CODE: 23212	Add to Cart Add to Compare List
Achromatopsia 3 - Sequence analysis of the entire coding region	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	Achromatopsia 3				CODE: 23213	Add to Cart Add to Compare List
Angelman Syndrome - Sequence analysis of the entire coding region	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	Angelman Syndrome	UBE3A,			CODE: 23214	Add to Cart Add to Compare List
APC-Associated Polyposis Conditions - Deletion/duplication analysis	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	APC-Associated Polyposis Conditions	APC,			CODE: 23216	Add to Cart Add to Compare List
APC-Associated Polyposis Conditions - Sequence analysis of the entire coding region	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	APC-Associated Polyposis Conditions	APC,			CODE: 23215	Add to Cart Add to Compare List
Beta-Propeller Protein-Associated Neurodegeneration - Sequence analysis of the entire coding region	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	Beta-Propeller Protein-Associated Neurodegeneration	WDR45,			CODE: 23217	Add to Cart Add to Compare List
BMPR1A-Related Juvenile Polyposis - Sequence analysis of the entire coding region	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	BMPR1A-Related Juvenile Polyposis	BMPR1A,			CODE: 23218	Add to Cart Add to Compare List
Carnitine Palmitoyltransferase IA Deficiency - Targeted mutation analysis	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	Carnitine Palmitoyltransferase IA Deficiency	CPT1A,	Targeted mutation analysis		CODE: 23219	Add to Cart Add to Compare List
CFTR-Related Disorders - Deletion/duplication analysis	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	CFTR-Related Disorders	CFTR,			CODE: 23222	Add to Cart Add to Compare List
CFTR-Related Disorders - Sequence analysis of the entire coding region	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	CFTR-Related Disorders	CFTR,			CODE: 23220	Add to Cart Add to Compare List
CFTR-Related Disorders - Targeted mutation analysis	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	CFTR-Related Disorders	CFTR,	Targeted mutation analysis		CODE: 23221	Add to Cart Add to Compare List
CNGB3-Related Stargardt Disease 1 - Sequence analysis of the entire coding region	Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center	CNGB3-Related Stargardt Disease 1	CNGB3,			CODE: 23223	Add to Cart Add to Compare List

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