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Maastricht University Medical Centre, Clinical Genomics

Disorder	Genes	Test Method	Lab Info	Product code
Achondroplasia - Deletion/duplication analysis	Maastricht University Medical Centre, Clinical Genomics	Achondroplasia	FGFR3,	Deletion/duplication analysis		CODE: 19882	Add to Cart Add to Compare List
Achondroplasia - Sequence analysis of the entire coding region	Maastricht University Medical Centre, Clinical Genomics	Achondroplasia	FGFR3,	Sequence analysis of the entire coding region		CODE: 19881	Add to Cart Add to Compare List
ACTC1-Related Dilated Cardiomyopathy - Sequence analysis of the entire coding region	Maastricht University Medical Centre, Clinical Genomics	ACTC1-Related Dilated Cardiomyopathy	ACTC1,	Sequence analysis of the entire coding region		CODE: 19883	Add to Cart Add to Compare List
ACTC1-Related Familial Hypertrophic Cardiomyopathy - Sequence analysis of the entire coding region	Maastricht University Medical Centre, Clinical Genomics	ACTC1-Related Familial Hypertrophic Cardiomyopathy		Sequence analysis of the entire coding region		CODE: 19884	Add to Cart Add to Compare List
ACVR2B-Related Visceral Heterotaxy - Sequence analysis of the entire coding region	Maastricht University Medical Centre, Clinical Genomics	ACVR2B-Related Visceral Heterotaxy	ACVR2B,	Sequence analysis of the entire coding region		CODE: 19885	Add to Cart Add to Compare List
Andersen Syndrome Type 1 - Sequence analysis of the entire coding region	Maastricht University Medical Centre, Clinical Genomics	Andersen Syndrome Type 1	KCNJ2,	Sequence analysis of the entire coding region		CODE: 19886	Add to Cart Add to Compare List
Angelman Syndrome - Deletion/duplication analysis	Maastricht University Medical Centre, Clinical Genomics	Angelman Syndrome	UBE3A,	Deletion/duplication analysis		CODE: 19890	Add to Cart Add to Compare List
Angelman Syndrome - Methylation analysis	Maastricht University Medical Centre, Clinical Genomics	Angelman Syndrome	UBE3A,	Methylation analysis		CODE: 19888	Add to Cart Add to Compare List
Angelman Syndrome - Sequence analysis of the entire coding region	Maastricht University Medical Centre, Clinical Genomics	Angelman Syndrome	UBE3A,	Sequence analysis of the entire coding region		CODE: 19887	Add to Cart Add to Compare List
Angelman Syndrome - Uniparental disomy study (UPD)	Maastricht University Medical Centre, Clinical Genomics	Angelman Syndrome	UBE3A,	Uniparental disomy study (UPD)		CODE: 19889	Add to Cart Add to Compare List
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy 5 - Sequence analysis of the entire coding region	Maastricht University Medical Centre, Clinical Genomics	Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy 5		Sequence analysis of the entire coding region		CODE: 19891	Add to Cart Add to Compare List
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy 8 - Sequence analysis of the entire coding region	Maastricht University Medical Centre, Clinical Genomics	Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy 8		Sequence analysis of the entire coding region		CODE: 19892	Add to Cart Add to Compare List

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