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- Svorio reguliavimo DNR tyrimas
- geneticGPS: Protėvių kilmės DNR tyrimas
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- geneticGPS: Protėvių kilmės DNR tyrimas
- Odos priežiūra pagal Jūsų DNR
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- Horse
- Coat Colour Pearl dilution
- Hyperpigmentation (Incontinentia pigmenti)
- Polysaccharide Storage Myopathy (patent owner)
- Night blindness / Coat colour Appaloosa pattern
- Coat colour Grey
- Coat Colour Overo-factor (OLWS)
- Coat Colour Agouti
- Parentage Verification Horse
- Coat Colour Cream dilution
- Severe Combined Immuno Deficiency (SCID)
- Paternity Verification Horse
- Malignant Hyperthermia (MH)
- Foal Immunodeficiency Syndrome
- Coat Colour Silver dilution
- Androgen Insensitivity Syndrome (AIS) 2
- Coat Colour Dun dilution
- Junctional Epidermolysis Bullosa 2 (JEB2)
- Myotonia
- Coat Colour Chestnut
- Coat Colour Champagne dilution
- Hoof wall separation disease (HWSD)
- Coat Colour Tobiano
- CombiBreed Genetic Diseases
- Maternity Verification Horse
- Coat Colour Macchiato (Splashed White)
- Thrombasthenia 1
- Glycogen Branching Enzyme Deficiency (GBED)
- Coat Colour White Spotting 3
- Coat Colour Dominant White 1
- Coat Colour Roan
- Androgen insensitivity syndrome (AIS)
- CombiBreed Coat Colour
- CombiBreed Genetic Diseases Plus
- CombiBreed SCID. CA. LFS. OAAM and DNA profile
- Coat Colour Sabino 1
- Lavender Foal Syndrome (LFS)
- Hydrocephaloid
- Cerebellar Abiotrophy (CA)
- Occipitoatlantoaxial Malformation (OAAM)
- DNA profile Horse
- Hyperkalemic Periodic Paralysis (HYPP)
- SynchroGait (DMRT3-Variants)
- Parentage Verification Zebra
- Coat Colour Appaloosa Pattern-1 (PATN1)
- Coat Colour Dominant White 3
- Coat Colour White Spotting 1
- Polysaccharide Storage Myopathy (partner lab)
- Dwarfism B4GALT7 (Friesian)
- Junctional Epidermolysis Bullosa 1 (JEB1)
- HERDA
- Dwarfism ACAN D1. D2. D3 improved. D4
- Parentage Verification Donkey
- Cattle
- Coat Colour Telstar-factor
- Fishy Off-Flavour (FMO3)
- Protoporphyria
- Coat Colour Redfactor
- Beta Lactoglobulin
- DUMPS
- Freemartinism
- FH2 mutation
- Robertsonian translocation / Karyotyping
- Double Muscling
- Polled
- Kappa Casein
- Double Muscling - Myostatin - 9 DNA-variants
- Mulefoot
- Cholesterol Deficiency (Holstein)
- Citrullinaemia
- FH4 mutation
- BLAD
- Achondrodysplasia (Dexter)
- Factor XI deficiency
- Beta Casein Protein Test (NON DNA)
- Complex Vertebral Malformation (CVM)
- Brachyspina Mutation Test
- Cat
- Progressive Retinal Atrophy (rdAc-PRA)
- Polycystic Kidney Disease (PKD)
- Hypotrichosis. with short life expectancy
- Porphyria. Acute Intermittent (4) 4
- Bloodtyping AB (DNA test Ragdoll Cats)
- Hereditary Myopathy
- Progressive Retinal Atrophy (Rdy-PRA)
- Hyperlipoproteinaemia
- Hair Length Norwegian Forest
- Sphynx. Hairless Coat
- Dihydropyrimidinase Deficiency
- Coat Colour Cinnamon
- Mucopolysaccharidosis VI
- CombiBreed Coat Colour
- Hypertrophic Cardio Myopathy 1 (HCM1)
- Periodic paralysis (WNK4 - Hypokalemia)
- Glycogentoxicosis GSD Type IV
- Gangliosidosis. GM2. GM2A
- Autoimmune Lymphoproliferative Syndrome (ALPS)
- Coat Colour Burmese
- CombiBreed Hair Length
- Coat colour Russet (Burmese)
- Porphyria. Acute Intermittent (4) 6
- Factor XII Deficiency
- Gangliosidosis. GM2. type II - 3
- Coat Colour E locus. extension
- Haemophilia B - 2
- Mucopolysaccharidosis VII (3)
- Congenital Adrenal Hyperplasia
- Hypothyroidism
- Gangliosidosis. GM2. type II - 1
- Alpha-Mannosidosis
- Parentage Verification Cat
- Niemann-Pick C1 Disease
- Porphyria. Acute Intermittent (4) 2
- Hair Length Ragdoll
- Coat Colour Agouti
- Gangliosidosis. GM2. type II - 2
- Hair Length all breeds
- Coat Colour Dilution
- Vitamin D-deficiency rickets. type I
- Bloodtyping AB (DNA test)
- Porphyria. Congenital Erythropoietic (2) 1
- Niemann-Pick Syndrome Type C1
- Mucopolysaccharidosis I
- Bloodtyping AB (Serology)
- Coat Colour Siamese
- Brachycephaly (Frontonasal Dysplasia (FND))
- Osteochondrodysplasia (Fold Mutation)
- Paternity Verification Cat
- Porphyria. Acute Intermittent (4) 1
- Mucopolysaccharidosis VII (2)
- Porphyria. Acute Intermittent (4) 5
- Hypertrophic Cardio Myopathy 3 (HCM3)
- Porphyria. Congenital Erythropoietic (2) 2
- Coat colour Dominant White & White Spotting
- Mucopolysaccharidosis VII
- Coat Colour Chocolate
- Gangliosidosis. GM1
- Haemophilia B - 1
- Spinal Muscular Atrophie (SMA)
- Pyruvaatkinase Deficiency (PKDef)
- Devon Rex. Curly Coat
- Porphyria. Acute Intermittent (4) 3
- DNA profile Cat
- Cornish Rex. Curly/woolly coat
- Feline Leukocyte Adhesion Deficiency (CD18. FLAD)
- Maternity Verification Cat
- Hair Length Maine Coon
- Hypotrichosis. with whiskers short and curled 1
- Hypertrophic Cardio Myopathy 2 (HCM2)
- CombiBreed Genetic Diseases
- Primary Hyperoxaluria II
- Dog
- Šunų genetinio profilio (DNR) tyrimas
- Dog_Spinal Dysraphism
- Degenerative Myelopathy 2 (DM2 Bernese mountain)
- Congenital Myasthenic Syndrome
- HNPK (partner lab)
- CombiBreed FCI Group 08
- Hyperuricemia (HUU)
- Hyperkeratosis. epidermolytic
- FN. Familial Nephropathy (partner lab)
- GM1
- prcd PRA (partnerlab)
- CMR2 (Canine Multifocal Retinopathy)
- C3 Deficiency
- CombiBreed FCI Group 09
- Primary Ciliary dyskinesia
- Musladin-Lueke syndrome (MLS)
- Cerebellar Abiotrophy (NCCD)
- Hypocatalasia
- CombiBreed FCI Group 10
- Haemophilia A (Factor VIII) (partner lab)
- Neuronal ceroid lipofuscinosis (NCL) 1
- CLAD. Type III
- Thrombopathia 2
- Juveniele Myoclonic Epilepsy
- Gangliosidosis. GM2. Type I (B variant)
- L2-HGA
- Maternity Verification Dog
- Myasthenia gravis-like disease
- Hereditary Cataract (HC) - HSF4
- Multifocal Retinopathy 3 (cmr3) 2
- Ectodermal Dysplasia X-linked
- Polyneuropathy 2
- Muscular hypertrophy (double muscling)
- Muscular Dystrophy. Duchenne Type (DMD)
- Neuronal ceroid lipofuscinosis (NCL) 2
- PRA 2
- CombiBreed FCI Group 07
- Polycystic kidney disease (PKD1)
- CombiBreed FCI Group 06
- Retinal Dysplasia Retinal Folds RD OSD 1
- Congenital Myasthenic Syndrome
- rcd1 PRA
- Nephritis
- Dilated Cardiomyopathy (DCM)
- CombiBreed FCI Group 05
- Bleeding disorder due to P2RY12 defect
- Osteogenesis imperfecta 2
- IGS (Selective Cobalamin Malabsorption) 2
- CombiBreed Border Collie
- Neuroaxonal Dystrophy
- Primary Hyperoxaluria
- Amelogenesis Imperfecta
- Narcolepsy 1
- Glycogen Storage Disease GSD I
- gPRA
- Congenital Cornification Disorder
- Neuronal ceroid lipofuscinosis (NCL) 10
- Mucopolysaccharidose Type VII - 2
- Exercise Induced Collapse. EIC (partner lab)
- Warburg Micro Syndrome 1 (WARBM1)
- Cerebellar Cortical Degeneration
- Coat Colour B-locus
- Von-Willebrands Disease Type 3
- FN. Familial Nephropathy (patent owner)
- Cystinuria I - A - 1
- Thrombasthenia
- Achromatopsia 3 (cone degeneration. hemeralopia)
- Haemophilia A (Factor VIII) (patent owner)
- Acute Respiratory Distress Syndrome (ARDS)
- Paternity Verification Dog
- X-SCID
- Coat Colour Merle (patent owner)
- Neonatal Encephalopathy
- Globoid Cell Leukodystrophy / Krabbes Disease
- Oculocutaneous Albinism
- Cystinuria. type II - A
- GR_PRA2
- CombiBreed FCI Group 01
- CombiBreed FCI Group 02
- Parentage Verification Dog
- Primary Glaucoma
- Muscular Dystrophy. Duchenne type (MDM)
- Cystinuria. type II - A - 1
- Pyruvatekinase Deficiency (PKDef) 2
- GR_PRA1
- Coat Colour Panda White Spotting
- MDR1 (partner lab)
- PRA
- rcd1a PRA
- Šunų kailio spalvos kombinuotas tyrimas
- Hyperkeratosis. palmoplantar
- Tremor. X-linked
- CombiBreed Labrador Retriever
- Sensory Neuropathy
- Improper Coat/Furnishings
- Polyneuropathy 1
- Coat Colour K-locus
- Hereditary Cataract 2 (HSF4)
- Ichthyosis 3
- SCID
- FBN2
- Neuronal ceroid lipofuscinosis (NCL) 6
- Polyneuropathy 4 (LPN2)
- SCID 2
- HNPK (patent owner)
- Muscular Dystrophy (GRMD)
- Multifocal Retinopathy 3 (cmr3) 1
- PFK (Phosphofructokinase Deficiency)
- PRA crdPRA
- Episodic Falling Disease (patent owner)
- Palmoplantar keratoderma 1 (FNEPPK1)
- Neuronal ceroid lipofuscinosis (NCL) 5 GR
- Cleft Lip / Palate and Syndactyly (CLPS)
- Cerebellar Ataxia (SDCA1)
- Spinocerebellar ataxia
- Congenital Hypothyroidism (CHG) 2
- Thrombopathia 3
- Dog_Skin Fragility
- Hypomyelination
- Maligne Hyperthermia
- Narcolepsy 2
- Ichthyosis 4
- Aberrant Autophagy (LSD)
- Exercise Induced Collapse. EIC (patent owner)
- Alexander Disease
- GSDII (Pompe Disease)
- Congenital Hypothyroidism (CHG) 3
- Hiplaxity 1
- Cone Rod Dystrophy 2 (crd2)
- Mucopolysaccharidosis Type VII
- Myotonia Congenita
- Coat Colour Saddle tan vs black-and-tan
- Coat Colour H-locus (Harlequin)
- Pyruvate kinase Deficiency (PKDef)
- Osteogenesis imperfecta
- Ichthyosis 2
- CombiBreed FCI Group 03
- Dry Eye Curly Coat Syndrome
- X Linked PRA1 (XL PRA1)
- Pyruvate Dehydrogenase Phosphatase 1 (PDP1)
- Thrombocytopaenia
- rcd4 PRA
- Cerebellar Ataxia / NCL-A
- Type A PRA
- Cone Degeneration
- Primary Lens Luxation (PLL)
- Achromatopsia 2 (cone degeneration. hemeralopia)
- Chondrodystrophy and Intervertebral Disc Disease
- Factor IX Deficiency
- Cerebellar Hypoplasia Resembling
- Centronuclear Myopathy (CNM. also known as HMLR)
- MTM
- Coppertoxicosis
- Cerebellar Ataxia
- IGS (Selective Cobalamin Malabsorption) 3
- Coat Colour Merle (partner lab)
- CombiBreed Australian Shepherd
- Cystinuria. type II - B
- Hair length
- Macular Corneal Dystrophy
- Prekallikrein deficiency
- Collie Eye Anomaly (CEA_CH. partnerlab)
- Neuronal ceroid lipofuscinosis (NCL) 5
- Coat Colour Piebald
- Myotonia Congenita 2
- Cone Rod Dystrophy 1 (crd1)
- CombiBreed German Shepherd
- Fucosidosis
- Collie Eye Anomaly (CEA_CH. patent owner Optigen)
- crd4-PRA (previously cord1-PRA)
- PRA erd
- IGS (Selective Cobalamin Malabsorption) 1
- Congenital Hypothyroidism (CHG) 1
- CLAD. Type I
- Polycythemia
- Trapped Neutrophil Syndrome (TNS)
- Gray Collie Syndrome (Cyclic Neutropenia)
- Neuronal ceroid lipofuscinosis (NCL) 8-2
- Von-Willebrands Disease Type 1
- Hiplaxity 2
- Adult Onset Neuropathy (AON)
- PAP-PRA1 2
- Mucopolysaccharidosis Type IIIa
- Glaucoma (POAG)
- Coat Colour Em-locus
- PAP-PRA1 1
- crd3
- Epilepsy. BFJ
- Congenital Myasthenic Syndrome 2
- Sensory Neuropathy 3
- Von-Willebrands Disease Type 2-2
- Dominant PRA
- CSNB (Congenital Stationary Night Blindness)
- Gallbladder Mucocele
- Dental Hypomineralization (Raine Syndrome)
- rcd2 PRA
- Pituitary dwarfism
- Vitamin D-deficiency rickets. type II
- CombiBreed Golden Retriever
- Narcolepsy 3
- Weight and Appetite in Obesity-Prone dogs
- Degenerative Myelopathy. DM (partner lab)
- Juvenile Laryngeal Paralysis Polyneuropathy (JLPP)
- Coat Colour D-Locus Improved (MLPH)
- Craniomandibular Osteopathy (CMO)
- Coat Colour E-locus
- Osteogenesis Imperfecta 3
- CMR1 (Canine Multifocal Retinopathy)
- Pyruvatekinase Deficiency (PKDef) 3
- Factor VII deficiency
- Thrombopathia
- Polyneuropathy 3 (LPN1)
- Limb girdle muscular dystrophy (LGMD) 1
- Gangliosidosis. GM2. type II
- Cerebellar Ataxia 2
- Brachyury (Bobtail)
- Thrombasthenia 2
- Skeletal Dysplasia 2 (SD2)
- Hemorragic diathesis (Scott Syndrome)
- Degenerative Myelopathy. DM (patent owner)
- Combination Pack Partnerlab
- Curly Coat
- Ichthyosis 5
- Spinocerebellar ataxia (2)
- Dermatofibrosis
- Retinal Dysplasia Retinal Folds RD OSD 2
- rcd3 PRA
- Von-Willebrands Disease Type 2
- Episodic Falling Disease (partner lab)
- Chondrodysplasia. Disproportionate Short-Limbed
- PRA BBS4
- PRA type 3
- Coat Colour A-locus
- Cerebellar Ataxia. progressive early-onset
- Epidermolysis bullosa. dystrophic (RDEB)
- CombiBreed FCI Group 04
- Von Willebrand disease 3 - 2
- prcd PRA (patent owner Optigen)
- Neuronal ceroid lipofuscinosis (NCL) 8-1
- Myopathy
- Pig
- CombiBreed Value
- CCKAR_179
- Materity Verification Pig
- Karyotyping
- CCKAR_471
- Calpastatin Codon 249 (CAST249)
- CombiBreed Quality
- CombiBreed All Markers
- Parentage Verification Pig
- MC4R
- IGF-2
- DNA profile Pig
- Susceptibility to Ecoli F18
- Rendement Napolitane (RN)
- Susceptibility to Ecoli K88ab
- CombiBreed Health
- Paternity Verification Pig
- Porcine Stress Syndrome (PSS)
- HMGA1
- Calpastatin Codon 638 (CAST638)
- PRKAG3
- Sheep & goat
- Bird
- Other species and food safety
- Horse
- Vėžio genetiniai tyrimai
- Apie Myriad laboratoriją
- Krūties vėžys
- Kiaušidžių vėžys
- Žarnyno vėžys
- Gimdos vėžys
- Plaučių vėžys
- Paveldima Melanoma
- Melanoma
- Kasos vėžys
- Prostatos vėžys
- Krūties ir kiaušidžių vėžys
- BRACAnalysis
- EndoPredict
- Žarnyno vėžys
- Colaris
- Colaris AP
- Odos vėžys
- Melaris
- Plaučių vėžys
- myPlan Lung
- Kasos vėžys
- Panexia
- Prostatos vėžys
- Prolaris
- Chemotoksiškumo valdymas
- TheraGuide 5-FU
- PTEN genas
- Prezeon
- BRACAnalysis: Paveldimo krūties ir kiaušidžių vėžio tyrimas
- COLARIS: Paveldimo storosios žarnos ir gimdos gleivinės vėžio tyrimas
- COLARIS AP: Genetinis adenomatozinės polipozės storosios žarnos vėžio sindromų tyrimas
- MELARIS: Paveldimos melanomos ir kasos vėžio tyrimas
- „myPlan™ Lung Cancer“ plaučių vėžio tyrimas
- PANEXIA: Paveldimo kasos vėžio tyrimas
- Prolaris: Prognostinis medicininis tyrimas prostatos vėžiui
- TheraGuide 5-FU: Personalizuotas individualios chemoterapijos tyrimas
- Personalizuotas medicininis tyrimas, leidžiantis įvertinti PTEN geno būklę.
- EndoPredict: PERSONALIZUOTAM KRŪTIES VĖŽIO GYDYMUI
- Kiti tyrimai
- Kontaktai
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