Advanced search

Search results

Products found: 224Search results

← Prev 1 2 3 4 5 6 7 8 Next → 2 - 16

bio.logis Center for Human Genetics

Disorder	Genes	Test Method	Lab Info	Product code
11-beta-Hydroxylase-Deficient Congenital Adrenal Hyperplasia - Sequence analysis of the entire coding region	bio.logis Center for Human Genetics	11-beta-Hydroxylase-Deficient Congenital Adrenal Hyperplasia	CYP11B1,			CODE: 3889	Add to Cart Add to Compare List
17-alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia - Deletion/duplication analysis	bio.logis Center for Human Genetics	17-alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia	CYP17A1,			CODE: 3891	Add to Cart Add to Compare List
17-alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia - Sequence analysis of the entire coding region	bio.logis Center for Human Genetics	17-alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia	CYP17A1,			CODE: 3890	Add to Cart Add to Compare List
21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia - Deletion/duplication analysis	bio.logis Center for Human Genetics	21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia	CYP21A2,			CODE: 3893	Add to Cart Add to Compare List
21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia - Sequence analysis of the entire coding region	bio.logis Center for Human Genetics	21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia	CYP21A2,			CODE: 3892	Add to Cart Add to Compare List
ABCC8-Related Hyperinsulinism - Deletion/duplication analysis	bio.logis Center for Human Genetics	ABCC8-Related Hyperinsulinism	ABCC8,			CODE: 3895	Add to Cart Add to Compare List
ABCC8-Related Hyperinsulinism - Sequence analysis of the entire coding region	bio.logis Center for Human Genetics	ABCC8-Related Hyperinsulinism	ABCC8,			CODE: 3894	Add to Cart Add to Compare List
Achondroplasia - Sequence analysis of the entire coding region	bio.logis Center for Human Genetics	Achondroplasia	FGFR3,			CODE: 3896	Add to Cart Add to Compare List
Acromesomelic Dysplasia, Hunter-Thompson Type - Sequence analysis of the entire coding region	bio.logis Center for Human Genetics	Acromesomelic Dysplasia, Hunter-Thompson Type	GDF5,			CODE: 3897	Add to Cart Add to Compare List
Acromesomelic Dysplasia, Maroteaux Type - Sequence analysis of the entire coding region	bio.logis Center for Human Genetics	Acromesomelic Dysplasia, Maroteaux Type	NPR2,			CODE: 3898	Add to Cart Add to Compare List
Alpha1-Antitrypsin Deficiency - Targeted mutation analysis	bio.logis Center for Human Genetics	Alpha1-Antitrypsin Deficiency	SERPINA1,	Targeted mutation analysis		CODE: 3899	Add to Cart Add to Compare List
Angelman Syndrome - Deletion/duplication analysis	bio.logis Center for Human Genetics	Angelman Syndrome	UBE3A,			CODE: 3903	Add to Cart Add to Compare List

← Prev 1 2 3 4 5 6 7 8 Next → 2 - 16

Loading...