Ua_genetik_engl_ohnepreis

Lab order
business hours: mo - fr: 8:00 - 19:00 h, sa: 9:00 - 13:00 h first name _______________________________________ fax/e-mail: _______________________________________ : ________________________________________________ I have checked animals identity and assure that samples are taken from the animals mentioned above.
____________________________________________ s _- ture / stamp veterinarian ____________________________________________________- animal 1:
___________________________ pedigree-no.: ___________________________ animal 2 / mother (parentage):
___________________________ pedigree-no.: animal 3 / potential father (parentage):
___________________________ pedigree-no.: credit card
_:__________________________________________________ invoice-no.: ____________________________________________________ _________________________________________________ exp. date: ________________________________________________ ______________________________________________ _______________________________________________ For accepting credit card we charge EUR 2,10 plus VAT.
Brachyury
Myostation mutation
Myotonia Congenita
Collie Eye Anomaly (CEA)
Narcolepsy
8120 performed by Optigen
(Rough,- Smooth Collie, Border Collie, Australian Shepherd, Lancashire Heeler, 8155 Neonatal Encephalopathy
CSNB / Night Blindness
Neuronal Ceroid Lipofuscinosis (NCL)
Cystinuria
PDP1 - Pyruvat Dehydrogenase Phosphatase 1
Deficiency
Degenerative Myelopathy
(all breeds)
8017 Phosphofructokinase Deficiency (PFKD)
(English Springer Spaniel, American Cocker Spaniel) EIC - Exercise Induced Collapse
(Labrador Retriever, Curly Coated Retriever, Chesapeake Bay Retriever)
8128 cord1-PRA
(Miniature Smoothhaired-, Longhaired Dachshund, English Springer Spaniel) Hereditary Myopathy (HMLR, CNM)
(Labrador Retriever)
prcd-PRA
Factor VII
performed by Optigen
(Beagle, Giant Schnauzer, Airedale Terrier, Scottish Deerhound, Alaskan Klee Kai) 8127 performed by partnerlab
8016 Fucosidosis
(ACS, American Eskimo Dog, Australian Cattle Dog, Australian Shepherd, Australian Stumpy Tail Cattle Dog, Chesapeake Bay Retriever, Chinese Crested, 8215 Osteogenesis imperfecta
ECS, Entlebucher Mountaindog, Finnish Lapphund, Golden Retriever, Kuvasz, Lapponian Herder, Labrador Retriever, Labradoodle, Nova Scotia Duck Tolling Retriever, Portuguese Waterdog, English Cocker Spaniel, 8007 Globoid Cell Leukodystrophy / Krabbe-disease
(West Highland White Terrier, Cairn Terrier) Swedish Lapphund, Toy Poodle, Dwarf Poodle) GM1-Gangliosidosis
Progressive Retinal Atrophy (crd-PRA)
Grey Collie Syndrome
Progressive Retinal Atrophy (PRA)
(Irish Setter, Welsh Corgi, English Mastiff, Bull Mastiff, Sloughi) GRMD (Muscular Dystrophy)
rcd2-PRA
GSDIIIa - Glycogen Storage Disease
Primary Lens Luxation (PLL)
(Chinese Crested, Jack Russell Terrier, Jagd Terrier, Lancashire Heeler, Miniature Bull Terrier, Parson Russell Terrier, Patterdale Terrier, Rat Terrier, Sealyham Terrier, Tibet Hemophilia B (Factor IX)
Terrier, Toy Fox Terrier, Volpino Italiano, Welsh Terrier) Hereditary Neuropathy
Pyruvatkinase Deficiency (PK Deficiency)
Hereditary Cataract
Retinal Dysplasia (OSD)
Hyperuricosuria
Trapped Neutrophil Syndrome (TNS)
Copper Toxicosis
von-Willebrand-Disease
Malignant Hyperthermia
von-Willebrand Disease Type 1
(Doberman Pinscher, German Pinscher, Manchester Terrier, Bernese Mountain Dog, Coton de Tulear, Drentsche Patrijschond, Kerry Blue Terrier, Papillon, Stabyhound, L-2-HGA (L-2-Hydroxyglutaric Aciduria)
MDR1 Gene Defect (Ivermectin Sensitivity)
von-Willebrand Disease Type 2
Collie, Shetland Sheepdog, Australian Shepherd, Bobtail, Longhaired Whippet, Silken (German Wirehaired Pointer, German Shorthaired Pointer) Windhound, American White Shepherd, Waeller, Mc Nab, German Shepherd) 8119 von-Willebrand Disease Type 3
Mucopolysaccharidosis Type VII (MPS)
Dwarfism
A-Locus (Agouti)
EM-Locus (Melanistic Mask Allele)
B-Locus (Coat Colour Brown)
Coat Length
D-Locus (Dilution)
E-Locus (Coat Colours Yellow, Lemon, Red, Cream,
K-Lokus (brindle)*
Apricot)
8180 Sable*
Parentage (each offspring)
likelihood ratio calculation (incl. DNA-Profile)
(breeds upon request)
DNA-Profile (each parent)
Breed Analysis (DNA-Profile + assignment)
(breeds upon request)
For parentage evaluation DNA profiles of every parent is needed.
Gangliosidosis GM 1 / GM 2
Hypertrophic Cardiomyopathy (HCM)
Glycogen Storage Disease (GSD) Type IV
Polycystic Kidney Disease (PKD)
GM2 Gangliosidosis
Progressive Retinal Atrophy (rdAc-PRA)
(Abyssinian, Somali, Ocicat, Siamese, Bengal, Balinese, Javanese, Oriental Shorthair, Hypertrophic Cardiomyopathy (HCM)
Mutation 1 Meurs (G --> C)(Maine Coon, Ragdoll)
8015 Pyruvatkinase Deficiency (PK)
8129 Hypertrophic Cardiomyopathy (HCM)
8123 Feline Spinal Muscular Atrophy (SMA)
Coat Colour Variant Agouti
Coat Colour Amber
Coat Colour Variant Burmese
Coat Colour Chocolate
Coat Colour Variant Siamese (Point)
Coat Colour Cinnamon
Coat Colour Variant Dilution
Coat Length
Genetic Determination of Blood Group
Serologic Evaluation of Blood Group
(all breeds except Turkish Angora, Ragdoll, Sibirian, Neva Masquerade, European Serologic evaluation of the blood group is needed to differentiate between groups A, B and AB. Prior to any blood transfusion both
donor and recipient should be tested to avoid incompatibilities. sample material: EDTA blood
Parentage (each offspring)
DNA-Profile (each parent)
Please send in samples from both parents even if only the parentage of the father has to be verified.
All animals with possible parenthood should be tested.
For parentage evaluation DNA profiles of every parent is needed.
gerichtsverwertbar sein soll.
# If only sample material from one parent is available we would like you to contact us prior to sending in the samples.
Cerebellar Abiotrophy (CA) Screening test
Hyperkalaemic Periodic Paralysis (HYPP)
Equine Malignant Hyperthermia
Lavender foal Syndrom (LFS)
GBED (Glycogen-Branching-Enzyme Deficiency)
PSSM (Polysaccharid-Storage-Myopathy Type I)
(Quarter Horse, American Paint Horse, Warmblood, Draft Breeds) Severe Combined Immunodeficiency (SCID)
(Hereditary Equine Regional Dermal Asthenia) (Quarter Horse) Lethal White Foal Syndrome (OLWS)
Coat Colour Black (Agouti)
Coat Colour Variant Pearl*
Coat Colour Variant Champagne
Coat Colour Variant Roan Zygosity*
Coat Colour Variant Cream / Dilution
Coat Colour Variant Sabino
Coat Colour Variant Dun Zygosity*
Coat Colour Variant Silver dapple
Coat Colour Chestnut
Coat Colour Variant Tobiano
8159 Graying
Parentage (each offspring)
DNA-Profile (each parent)
. r die Vaterschaft geklärt werden
d .in Betracht kommender Väter.
d. il die Erstellung eines DNA-Profils nötig.
gerichtsverwertbar sein soll.
d .ing in the samples.
1) The identity of the animal needs to be confirmed by a veterinarian (specification by microchip-no, tattoo-no. or pedigree-no.) 2) Certificates are not issued for partner laboratory services and genetic blood group of cats 3) Certificates are included in the services of DNA-profile and parentage testing In order to allow the breeding club discount please enclose a breeding club member confirmation to each
sample submission. The invoice will not be altered subsequently.
General conditions of business:
net prices in Euro / If the invoice is sent to the owner we charge x 1.3
/ All statements according to our conditions see www.laboklin.com / All terms and prices are subject to changes.
015.003 10/11

Source: http://essclub.cz/zdravi/fuco-cord1/fuco-cord1_laboklin-en_form.pdf