Login
0
Dr. van Haeringen Laboratorium B.V.
en
Nederland
Nederlands
English
Other countries
English
Deutsch
Nederlands
Other countries
English
Nederlands
België/Belgique
Français
Nederlands
English
Deutschland
Deutsch
English
España
Español
France
Français
Lietuva
Lietuvių
Nederland
Nederlands
English
Norge
Norsk, Bokmål
Webshop
Dog
Cat
Horse
Checkout
My CombiBreed
Info results
Results and inheritance
Interpretation testresults
Test specifics
Coat colour and variation
Dog
Cat
Horse
Parentage verification
Service
Sample submission forms
Request form swab / bags
News
FAQ
Contact
About us
Search test(s) for your breed
Breed
Include tests which are not breed specific
Horse
Genome Scan
P623
Equine SNP70 (GeneSeek)
Kinship, Parentage and Identity
P205
DNA profile Horse
P263
DNA profile Horse - Germany
P266
DNA profile Horse - Icelandic
P202
Maternity Verification Horse
P261
Maternity Verification Horse - Germany
P264
Maternity Verification Horse - Icelandic
P216
Parentage Verification Donkey
P200
Parentage Verification Horse
P251
Parentage Verification Horse - Germany
P253
Parentage Verification Horse - Icelandic
P220
Parentage Verification Zebra
P201
Paternity Verification Horse
P262
Paternity Verification Horse - Germany
P265
Paternity Verification Horse - Icelandic
Combination Packages
P324
CombiBreed 5-panel Quarter Horse & related breeds
P325
CombiBreed 6-panel Quarter Horse & related breeds
P858
CombiBreed Arabian
P322
CombiBreed Barock Pinto
P404
CombiBreed Coat Colour
P323
CombiBreed Falabella
P508
Combibreed Friesian
P307
CombiBreed Genetic Diseases
Genetic diseases
P506
Androgen insensitivity syndrome (AIS)
P309
Androgen Insensitivity Syndrome (AIS) 2
P802
Cerebellar Abiotrophy (CA)
P387
Distichiasis
P306
Dwarfism ACAN D1, D2, D3 improved, D4
P381
Dwarfism B4GALT7 (Friesian)
P839
Foal Immunodeficiency Syndrome
P791
Glycogen Branching Enzyme Deficiency (GBED)
P786
HERDA
P899
Hoof wall separation disease (HWSD)
P519
Hydrocephaloid
P705
Hyperkalemic Periodic Paralysis (HYPP)
P655
Hyperpigmentation (Incontinentia pigmenti)
P735
Junctional Epidermolysis Bullosa 1 (JEB1)
P877
Junctional Epidermolysis Bullosa 2 (JEB2)
P854
Lavender Foal Syndrome (LFS)
P926
Malignant Hyperthermia (MH)
P882
Myotonia
P311
Night blindness / Coat colour Appaloosa pattern
P314
Occipitoatlantoaxial Malformation (OAAM)
P385
Ocular squamous cell carcinoma (SCC)
P678
Polysaccharide Storage Myopathy 1
P803
Polysaccharide Storage Myopathy 1 (Patent Lab)
P704
Severe Combined Immuno Deficiency (SCID)
P507
Thrombasthenia 1
P318
Warmblood Fragile Foal Syndrome (WFFS)
Test on demand
P317
Curly hair
Other genetic traits
P907
Coat Colour Agouti
P305
Coat Colour Appaloosa Pattern-1 (PATN1)
P383
Coat Colour Camarillo White - W4
P853
Coat Colour Champagne dilution
P904
Coat Colour Chestnut
P713
Coat Colour Cream dilution
P592
Coat Colour Dominant White - W20
P591
Coat Colour Dominant White 1
P660
Coat Colour Dun dilution (External Patent Lab)
P807
Coat colour Grey
P902
Coat Colour Overo-factor (OLWS)
P783
Coat Colour Pearl dilution
P659
Coat Colour Roan
P785
Coat Colour Sabino 1
P784
Coat Colour Silver dilution / MCOA
P384
Coat Colour Snowdrop
P903
Coat Colour Tobiano
P512
Splashed white 1
P513
Splashed white 2
P514
Splashed white 3
Dog
Cat
Horse