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Praxis fuer Humangenetik Wien

Disorder Genes Test Method Lab Info Product code  
Praxis fuer Humangenetik Wien 11-beta-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP11B1, Sequence analysis of the entire coding region
Praxis fuer Humangenetik Wien 17-alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP17A1, Deletion/duplication analysis
Praxis fuer Humangenetik Wien 17-alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP17A1, Sequence analysis of the entire coding region
Praxis fuer Humangenetik Wien 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Deletion/duplication analysis
Praxis fuer Humangenetik Wien 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Sequence analysis of the entire coding region
Praxis fuer Humangenetik Wien 22q11.2 Deletion Syndrome Deletion/duplication analysis
Praxis fuer Humangenetik Wien 3-beta-Hydroxysteroid Dehydrogenase-Deficient Congenital Adrenal Hyperplasia HSD3B2, Sequence analysis of the entire coding region
Praxis fuer Humangenetik Wien 3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency HADH, Sequence analysis of the entire coding region
Praxis fuer Humangenetik Wien Abetalipoproteinemia MTTP, Sequence analysis of the entire coding region
Praxis fuer Humangenetik Wien Acute Intermittent Porphyria HMBS, Sequence analysis of the entire coding region
Praxis fuer Humangenetik Wien ACVRL1-Related Hereditary Hemorrhagic Telangiectasia ACVRL1, Sequence analysis of the entire coding region
Praxis fuer Humangenetik Wien Adrenoleukodystrophy, X-Linked ABCD1, Sequence analysis of the entire coding region
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