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Molecular Genetic Testing
5-Fluorouracil (5-FU)-Related Toxicity (DPD , Dihydropyridine Dehydrogenase Mutation)
Adipositas (Inherited Predisposition to Obesity)
Alpha1- Antitrypsin Deficiency ( S and Z mutations)
Alzheimer´s Disease (AD)
Apolipoprotein A-I-Deficiency
Asthma
Azoospermia (Congenital Bilateral Absence of Vas Dference, CBACD)
Breast Cancer, hereditary
Colon Cancer, hereditary non polyposis (HNPCC)
Colon Cancer, Hereditary Non Polyposis (HNPCC): Microsatellite Instability (MSI) for Cancer Detection and Familial Predisposit
Congenital Adrenal Hyperplasia (21-hydroxylase deficiency, AGS)
Cystic Fibrosis (Mucoviscidosis)
Factor V Leiden - Mutation (Inherited Predisposition to Thrombosis)
Familal Hypercholesterolemia (FH)
Familial Hyperlipoproteinemia Typ III (Dysbetalipoproteinemia)
Familial Nonhemolytic Hyperbilirubinemia (Gilbert`s Syndrome) / Irinotecan Toxicity
Fragile X Syndrome
Genetic forms of Malformation (Mutation Screening in the GLI3-Gene)
Genetic Predisposition to Bile-Stones (Cholelithiasis)
Hereditary Hemochromatosis
Hyperhomocysteinemia (Methylene-tetrahydrofolate-reductase - Deficiency, MTHFR)
Lactose Intolerance
Loss of Function of Hepatic Lipase (LIPC)
Muscle Dystrophy, Type Duchenne and Becker (DMD)
Myeloproliferative disorders (JAK2-mutation)
Osteoporosis
Prader-Willi-/ Angelman-Syndrome
Prothrombin Mutation / Deep-Vein Thrombosis
Silver-Russell-Syndrome
Uniparental Disomy (UPD1, UPD7, UPD14, UPD15)
Y chromosomal microdeletion (infertility testing)
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