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Comprehensive coagulation Panel (ECS014)
von Willebrand disease, vWD (ECB019)
Factor VII Deficiency (ECB020)
Canine blood typing (ECB055)
Progressive retinal atrophy (GCB001)
Primarily lens luxation (GCB002)
Degenerative myelopathy (GCB003)
Hyperuricosuria (GCB004)
Centronuclear myopathy (GCB005)
Exercise-Induced collapse (GCB006)
Hereditary nasal parakeratosi (GCB007)
Malignant hyperthermia (GCB008)
Neuronal ceroid lipofuscinosis (GCB009)
Musladin-lueke syndrome (GCB010)
Neonatal cerebellar cortical degeneration (GCB011)
Osteogenesis imperfecta (GCB012)
Primary open angle glaucoma (GCB013)
Ichthyosis (GCB014)
Muscular dystrophy (GCB015)
Neonatal encephalopathy (GCB016)
Pyruvate kinase deficiency (GCB017)
Juvenile hereditary cataracts (GCB018)
von Willebrand disease, vWD (GCB018)
Factor VII Deficiency (GCB018)
Multidrug Resistance 1 Mutation, MDR1 (GCB018)
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