Dagdrivarn.se

Lab order
Customer-No.
LABOR FÜR KLINISCHE DIAGNOSTIK GMBH & CO. KG hereditary diseases
Postfach 1810 · D-97668 Bad KissingenTelefon + 49 971/72020 · Telefax + 49 971/68546 business hours: monday - friday: 8.00 - 18.00 h dates of animals:
animal 1
M dog M cat M horse M cattle breed :
dates of animals:
animal 2
M dog M cat M horse M cattle breed :
dates of animals:
animal 3
M dog M cat M horse M cattle breed :
tests see next page
1st.report / desire:
We accept Visa and Mastercard
For accepting credit card we charge EUR 2,10 plus vat.
hereditary diseases
dog
M 8012 CLAD (Irish Setter)
M 8011 CSNB / night blindness (Briard)
M 8013 Cystinurie (Newfoundland, Landseer)
M 8023 Coat Colour brown (Labrador, Flatcoated Retriever, Doberman Pinscher, Poodle, Newfoundland, Galgo Español, Border Collie, Cocker Spaniel)
M 8126 Coat Colour cream,red,white,apricot (Poodle)
M 8018 Coat Colour yellow (Labrador, Flatcoated Retriever)
M 8026 Coat Colour brown and yellow (Labrador, Flatcoated Retriever)
M 8016 Fucosidosis (English Springer Spaniel)
M 8007 Globoid Zell Leucodystrophy / Krabbe-disease (Westhighland White Terrier, Cairn Terrier)
M 8000 Copper Toxicosis (Bedlington Terrier)
M 8022 Myotonia congenita (Miniature Schnauzer)
M 8017 Phosphofructokinase deficiency (PFK deficiency) (English Springer Spaniel)
M 8002 Progressive Retinal Atrophy (PRA) (Irish Setter, Welsh Corgi, Engl.-Bull Mastiff, Sloughi)
prcd-PRA (American-, English Cocker Spaniel, Chinese Crested, Entlebuch Mountain dog, Kuvasz, Lapponian Herder, Labrador Retriever, Miniature-, Toy Poodle, Swedish-, Finnish Lapp dog, other breeds on request)
M 8094 with Optigen Certificate (test run at Optigen)*
M 8127 without Optigen Certificate (test run at partnerlab)*
M 8104 Pyruvat Dehydrogenase Phosphatase 1 Deficiency (Sussex, Clumber Spaniel)
M 8015 Pyruvatkinase deficiency (PK deficiency) (Basenji, Westhighland White Terrier))
M 8119 von-Willebrand disease type I (Doberman Pinscher, Poodle, Manchester Terrier, Bernese Mountain Dog, Pembroke Welsh Corgi, German Pinscher, Kerry Blue Terrier)
M 8014 von-Willebrand disease type II (Deutsch Drahthaar)
M 8014 von-Willebrand disease type III (Scotch Terrier, Sheltie)
M 8063 X-SCID (Basset, Welsh Corgi)
M 8032 MDR1 gene defect / Ivermectin sensitivity (Collie, Sheltie, Austr. Sheperd, Longhaired Whippet, Silken Windhound, American White Shepherd, Waeller, Bobtail)
M 8062 Malignant Hyperthermia (all breeds)
M 8067 Narcolepsy (Dobermann, Labrador Retriever)
M 8066 GM1-Gangliosidosis (Husky)
M 8068 Golden Retriever muscular dystrophy (GRMD) (Golden Retriever)
M 8069 Mucopolysaccharidosis type VII (MPS) (German Sheperd)
M 8073 Hereditary Myopathy of Labrador Retrievers (HMLR) (Labrador Retriever)
M 8075 Neuronal Ceroid Lipofuscinosis (NCL) (Border Collie, American Bulldog)
M 8077 Coat Colour lemon (Dalmatian)
M 8079 Coat Colour lemon and brown (Dalmatian)
M 8098 Grey Collie Syndrome / Canine Cyclic Neutropenia (Collie)
M 8120 Collie Eye Anomaly (CEA) (Collie)*
M 8124 Coat Length (all breeds)
M 8125 L-2-HGA (L-2-hydroxyglutaric aciduria) (Staffordshire Bull Terrier)
M 8128 cord1-PRA (English Springer Spaniel, Miniature Long-Haired and Smooth-Haired Dachshund)
M 8131 Familial Nephropathy (FN) (English Cocker Spaniel)
cat
M 8013 Polycystic kidney disease (PKD) (Persian and Persian related breeds)
M 8002 Gangliosidosis Gm1 / Gm2 (Korat, Siamese)
M 8015 Pyruvatkinase deficiency (PK deficiency) (Abessinians, Somali)
M 8080 Hypertrophic cardiomyopathy (HCM) (Maine Coon) Mutation 1 (G --> C) Meurs
M 8129 Hypertrophic cardiomyopathy (HCM) (Maine Coon) Mutation 2 (G --> A) Koch
M 8116 Hypertrophic cardiomyopathy (HCM) (Ragdoll)
M 8117 Progressive Retinal Atrophy (rdAc-PRA) (Abessinians, Somali)
M 8083 Coat Colour cinnamon (all breeds)
M 8084 Coat Colour chocolate (all breeds)
M 8090 Coat Colour variant agouti (all breeds)
M 8085 Coat Colour variant Siamese (Point) (all breeds)
M 8086 Coat Colour Burmese brown (all breeds)
M 8099 Dilution (all breeds)
M 8113 Glycogen Storage Disease Type IV (Norwegian Forest Cat)
M 8121 Genetic Determination of blood group (all breeds except Ragdolls and Wildcats)
M 8123 Feline Spinal Muscular Atrophy (SMA) (Maine Coon)
horse
M 8016 Coat Colour chestnut (all breeds)
M 8000 Hyperkalaemic Periodic Paralysis (HYPP) (Quarter Horse, horses with QH blood))
M 8061 Lethal White Foal Syndrome (LWO) (Frame Overo)
M 8001 Severe Combined Immunodeficiency (SCID) (Arabian)
M 8070 Coat Colour black (Agouti) (all breeds)
M 8071 Coat Colour cream / dilution (all breeds)
M 8072 Herlitz junctional epidermolysis bullosa (H-JEB) (French draft horse)
M 8130 Tobiano (Tinker, Paint, Pinto)
cattle
M 8001 Bovine Leucocyte Adhesion deficiency (BLAD) (Holstein cattle)
M 8112 Marker test for meat quality (Angus cattle) *
pig
M 8062 MHS (all breeds)
Very important:
Optimal rehearsing material has a blood test. Please contact your veterinarian to this.
The rehearsing recipient should be allowed to be sent officially or to function as an official rehearsing recipient if the result shall be
court usuable.
In case of doubt connect your breeders association which is responsible for your animal, please.
March 2008 / All statements according to our conditions / all terms and prices are subject to changes. / * Partnerlab

Source: http://www.dagdrivarn.se/INFO/lab_order_genetic_sine.pdf