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Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division

Disorder	Genes	Test Method	Lab Info	Product code
Angelman Syndrome - Methylation analysis	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	Angelman Syndrome	UBE3A,	Methylation analysis		CODE: 26489	Add to Cart Add to Compare List
Cardiovascular Disease Risk Factor (Apolipoprotein E) - Targeted mutation analysis	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	Cardiovascular Disease Risk Factor (Apolipoprotein E)	APOE,	Targeted mutation analysis		CODE: 26490	Add to Cart Add to Compare List
CFTR-Related Disorders - Targeted mutation analysis	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	CFTR-Related Disorders	CFTR,	Targeted mutation analysis		CODE: 26491	Add to Cart Add to Compare List
Factor V Leiden Thrombophilia - Targeted mutation analysis	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	Factor V Leiden Thrombophilia	F5,	Targeted mutation analysis		CODE: 26492	Add to Cart Add to Compare List
FMR1-Related Disorders - Targeted mutation analysis	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	FMR1-Related Disorders	FMR1,	Targeted mutation analysis		CODE: 26493	Add to Cart Add to Compare List
GJB2-Related DFNB 1 Nonsyndromic Hearing Loss and Deafness - Sequence analysis of the entire coding region	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	GJB2-Related DFNB 1 Nonsyndromic Hearing Loss and Deafness		Sequence analysis of the entire coding region		CODE: 26494	Add to Cart Add to Compare List
GJB6-Related DFNB 1 Nonsyndromic Hearing Loss and Deafness - Targeted mutation analysis	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	GJB6-Related DFNB 1 Nonsyndromic Hearing Loss and Deafness		Targeted mutation analysis		CODE: 26495	Add to Cart Add to Compare List
HFE-Associated Hereditary Hemochromatosis - Targeted mutation analysis	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	HFE-Associated Hereditary Hemochromatosis	HFE,	Targeted mutation analysis		CODE: 26496	Add to Cart Add to Compare List
MECP2-Related Disorders - Sequence analysis of the entire coding region	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	MECP2-Related Disorders	MECP2,	Sequence analysis of the entire coding region		CODE: 26497	Add to Cart Add to Compare List
MTHFR Thermolabile Variant - Targeted mutation analysis	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	MTHFR Thermolabile Variant	MTHFR,	Targeted mutation analysis		CODE: 26498	Add to Cart Add to Compare List
Prader-Willi Syndrome - Methylation analysis	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	Prader-Willi Syndrome		Methylation analysis		CODE: 26499	Add to Cart Add to Compare List
Prothrombin-Related Thrombophilia - Targeted mutation analysis	Providence Sacred Heart Medical Center and Children's Hospital, Department of Laboratory Medicine/Molecular Diagnostic Division	Prothrombin-Related Thrombophilia	F2,	Targeted mutation analysis		CODE: 26500	Add to Cart Add to Compare List

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