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Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory

Disorder	Genes	Test Method	Lab Info	Product code
Angelman Syndrome - Deletion/duplication analysis	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	Angelman Syndrome	UBE3A,	Deletion/duplication analysis		CODE: 11701	Add to Cart Add to Compare List
Angelman Syndrome - Methylation analysis	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	Angelman Syndrome	UBE3A,	Methylation analysis		CODE: 11699	Add to Cart Add to Compare List
Angelman Syndrome - Uniparental disomy study (UPD)	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	Angelman Syndrome	UBE3A,	Uniparental disomy study (UPD)		CODE: 11700	Add to Cart Add to Compare List
Ashkenazi Jewish Carrier Multi-Gene Panels	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	Ashkenazi Jewish Carrier Multi-Gene Panels				CODE:	Add to Compare List
Cardiovascular Disease Risk Factor (Apolipoprotein E) - Targeted mutation analysis	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	Cardiovascular Disease Risk Factor (Apolipoprotein E)	APOE,	Targeted mutation analysis		CODE: 11702	Add to Cart Add to Compare List
CFTR-Related Disorders - Linkage analysis	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	CFTR-Related Disorders	CFTR,	Linkage analysis		CODE: 11704	Add to Cart Add to Compare List
CFTR-Related Disorders - Targeted mutation analysis	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	CFTR-Related Disorders	CFTR,	Targeted mutation analysis		CODE: 11703	Add to Cart Add to Compare List
Charcot-Marie-Tooth Neuropathy Type 1A - Targeted mutation analysis	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	Charcot-Marie-Tooth Neuropathy Type 1A	PMP22,	Targeted mutation analysis		CODE: 11705	Add to Cart Add to Compare List
FMR1-Related Disorders - Linkage analysis	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	FMR1-Related Disorders	FMR1,	Linkage analysis		CODE: 11707	Add to Cart Add to Compare List
FMR1-Related Disorders - Methylation analysis	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	FMR1-Related Disorders	FMR1,	Methylation analysis		CODE: 11708	Add to Cart Add to Compare List
FMR1-Related Disorders - Targeted mutation analysis	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	FMR1-Related Disorders	FMR1,	Targeted mutation analysis		CODE: 11706	Add to Cart Add to Compare List
GJB2-Related DFNA 3 Nonsyndromic Hearing Loss and Deafness - Sequence analysis of the entire coding region	Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory	GJB2-Related DFNA 3 Nonsyndromic Hearing Loss and Deafness		Sequence analysis of the entire coding region		CODE: 11709	Add to Cart Add to Compare List

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