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GENETAQ, Molecular Genetics Centre

Disorder	Genes	Test Method	Lab Info	Product code
11-beta-Hydroxylase-Deficient Congenital Adrenal Hyperplasia - Sequence analysis of the entire coding region	GENETAQ, Molecular Genetics Centre	11-beta-Hydroxylase-Deficient Congenital Adrenal Hyperplasia	CYP11B1,	Sequence analysis of the entire coding region		CODE: 14512	Add to Cart Add to Compare List
21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia - Deletion/duplication analysis	GENETAQ, Molecular Genetics Centre	21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia	CYP21A2,	Deletion/duplication analysis		CODE: 14515	Add to Cart Add to Compare List
21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia - Sequence analysis of the entire coding region	GENETAQ, Molecular Genetics Centre	21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia	CYP21A2,	Sequence analysis of the entire coding region		CODE: 14513	Add to Cart Add to Compare List
21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia - Targeted mutation analysis	GENETAQ, Molecular Genetics Centre	21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia	CYP21A2,	Targeted mutation analysis		CODE: 14514	Add to Cart Add to Compare List
22q11.2 Deletion Syndrome - Deletion/duplication analysis	GENETAQ, Molecular Genetics Centre	22q11.2 Deletion Syndrome		Deletion/duplication analysis		CODE: 14516	Add to Cart Add to Compare List
3-beta-Hydroxysteroid Dehydrogenase-Deficient Congenital Adrenal Hyperplasia - Sequence analysis of the entire coding region	GENETAQ, Molecular Genetics Centre	3-beta-Hydroxysteroid Dehydrogenase-Deficient Congenital Adrenal Hyperplasia	HSD3B2,	Sequence analysis of the entire coding region		CODE: 14517	Add to Cart Add to Compare List
3-Methylglutaconic Aciduria Type 1 - Sequence analysis of the entire coding region	GENETAQ, Molecular Genetics Centre	3-Methylglutaconic Aciduria Type 1	AUH,	Sequence analysis of the entire coding region		CODE: 14518	Add to Cart Add to Compare List
Aarskog Syndrome - Sequence analysis of the entire coding region	GENETAQ, Molecular Genetics Centre	Aarskog Syndrome	FGD1,	Sequence analysis of the entire coding region		CODE: 14519	Add to Cart Add to Compare List
ABCA4-Related Retinitis Pigmentosa - Sequence analysis of the entire coding region	GENETAQ, Molecular Genetics Centre	ABCA4-Related Retinitis Pigmentosa		Sequence analysis of the entire coding region		CODE: 14520	Add to Cart Add to Compare List
ABCB11-Related Intrahepatic Cholestasis - Sequence analysis of the entire coding region	GENETAQ, Molecular Genetics Centre	ABCB11-Related Intrahepatic Cholestasis		Sequence analysis of the entire coding region		CODE: 14521	Add to Cart Add to Compare List
ABCC8-Related Hyperinsulinism - Sequence analysis of the entire coding region	GENETAQ, Molecular Genetics Centre	ABCC8-Related Hyperinsulinism	ABCC8,	Sequence analysis of the entire coding region		CODE: 14522	Add to Cart Add to Compare List
ABCC8-Related Hyperinsulinism - Targeted mutation analysis	GENETAQ, Molecular Genetics Centre	ABCC8-Related Hyperinsulinism	ABCC8,	Targeted mutation analysis		CODE: 14523	Add to Cart Add to Compare List

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