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Products found: 148Search results

Center for Human Genetics Freiburg, Kohlhase Laboratory

Disorder Genes Test Method Lab Info Product code  
Center for Human Genetics Freiburg, Kohlhase Laboratory 22q11.2 Deletion Syndrome Deletion/duplication analysis
Center for Human Genetics Freiburg, Kohlhase Laboratory ABCA12-Related Autosomal Recessive Congenital Ichthyosis ABCA12, Deletion/duplication analysis
Center for Human Genetics Freiburg, Kohlhase Laboratory ABCA12-Related Autosomal Recessive Congenital Ichthyosis ABCA12, Sequence analysis of the entire coding region
Center for Human Genetics Freiburg, Kohlhase Laboratory Absence of Ulna and Fibula with Severe Limb Deficiency WNT7A, Deletion/duplication analysis
Center for Human Genetics Freiburg, Kohlhase Laboratory Absence of Ulna and Fibula with Severe Limb Deficiency WNT7A, Sequence analysis of the entire coding region
Center for Human Genetics Freiburg, Kohlhase Laboratory ACTA2-Related Thoracic Aortic Aneurysms and Aortic Dissections ACTA2, Deletion/duplication analysis
Center for Human Genetics Freiburg, Kohlhase Laboratory ACTA2-Related Thoracic Aortic Aneurysms and Aortic Dissections ACTA2, Sequence analysis of the entire coding region
Center for Human Genetics Freiburg, Kohlhase Laboratory ALOX12B-Related Autosomal Recessive Congenital Ichthyosis ALOX12B, Sequence analysis of the entire coding region
Center for Human Genetics Freiburg, Kohlhase Laboratory ALOXE3-Related Autosomal Recessive Congenital Ichthyosis ALOXE3, Sequence analysis of the entire coding region
Center for Human Genetics Freiburg, Kohlhase Laboratory Bruck Syndrome 2 PLOD2, Sequence analysis of the entire coding region
Center for Human Genetics Freiburg, Kohlhase Laboratory CHARGE Syndrome CHD7, Deletion/duplication analysis
Center for Human Genetics Freiburg, Kohlhase Laboratory CHARGE Syndrome CHD7, Sequence analysis of the entire coding region
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