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Products found: 69Search results

University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab

Disorder Genes Test Method Lab Info Product code  
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Deletion/duplication analysis
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Sequence analysis of the entire coding region
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab Angelman Syndrome UBE3A, Deletion/duplication analysis
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab Angelman Syndrome UBE3A, FISH-metaphase
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab Angelman Syndrome UBE3A, Methylation analysis
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab Angelman Syndrome UBE3A, Sequence analysis of the entire coding region
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab Angelman Syndrome UBE3A, Uniparental disomy study (UPD)
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab CFTR-Related Disorders CFTR, Deletion/duplication analysis
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab CFTR-Related Disorders CFTR, Mutation scanning of the entire coding region
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab CYP1B1-Related Primary Congenital Glaucoma Sequence analysis of the entire coding region
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab DFNA 6/14/38 Nonsyndromic Hearing Loss and Deafness Sequence analysis of select exons
University Hospital of Antwerp, Department of Medical Genetics - Wuyts Lab DFNA 9 Nonsyndromic Hearing Loss and Deafness Sequence analysis of select exons
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