OUR BREEDERS
All of our breeders undergo genetic health testing to ensure they produce the healthiest puppies possible!

Dixie Magnolia's
​Mardi Gras Parti On Bourbon
​(sire)

Mardi Gras is a 27 lb. medium size black and white parti colored F3 Third Generation Doubledoodle with a wavy fleece low shed coat.
He is 17” at the shoulder and 19” long.
He is half Labradoodle and half Goldendoodle.
​He is 2 years old.
He will be the start of our smaller size doodles.
He is super laid back and is so easy going. He is very sociable and well mannered.
He is currently in a wonderful guardian home.
​
Genetic Testing:
(all clear)
*Centronuclear Myopathy
*Cystinuria
*Degenerative
Myelopathy
*Exercise-
induced Collapse
*Myotubular Myopathy 1
*Narcolepsy
*Neonatal Encephalopathy with Seizures
*Progressive Retinal Atrophy
*Progressive Rod Cone Degeneration
*Retinal Dysplasia/
Oculoskeletal
Dysplasia 1
​*Von Willebrand Disease

​

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Dixie Magnolia's Mardi Gras
​Parti on Bourbon

Dixie Magnolia's
​Beignet Au Lait In The Square
​(dam)

​​Beignet is a 60 lb. F2 Third Generation caramel colored Goldendoodle with a
​ wavy low shed coat.
She is 24” at the shoulderand 26” long.
She is 2 years old.
She has the typical sweet Golden Retriever personality and always greets you with her favorite toy in her mouth. And she LOVES playing in the water!
​
Genetic Testing:
(all clear)
*Degenerative Myelopathy
*Ichthyosis (Golden Retriever Type)
*Neonatal Encephalopathy with Seizures
*Progressive Retinal Atrophy, Golden Retriever 1
*Progressive Retinal Atrophy, Golden Retriever 2
*Progressive Retinal Atrophy,
*Progressive Rod-Cone Degeneration
*Von Willebrand Disease I
*Von Willebrand Disease II

Dixie Magnolia's French Market Beignet Au lait

Dixie Magnolia's
​ Cajun Reaux
(dam)

Reaux is a 38 lb. F1b Second Generation chocolate colored Labradoodle with a curly
​ wool non shedding coat
She is 4 years old
She has produced two litters of outstanding puppies with Gumbeaux and is the best mother to her puppies anyone could ever ask for.
Registered through Continental Kennel Club
​
Genetic Testing:
​(all clear)
*Centronuclear Myopathy
*Cystinuria
*Degenerative Myelopathy
*Exercise-induced Collapse
*Myotubular Myopathy 1
*Narcolepsy
*Neonatal Encephalopathy with Seizures
*Progressive Retinal Atrophy
*Progressive Rod Cone
Degeneration
*Retinal Dysplasia/
Oculoskeletal Dysplasia 1
​*Von Willebrand Disease
​Hips: OFA Good
Elbows: OFA Normal

Dixie Magnolia's
​ Cajun Reaux

Dixie Magnolia's
​ Cajun ​Gumbeaux
(sire)

Gumbeaux is a 65 lb. F1b Second Generation chocolate parchment and white parti Labradoodle, with a soft, curly fleece non shedding coat. He has the most beautiful amber colored eyes that are hypnotic. He has produced three outstandling litters of puppies so far.
​He is 4 years old.
Registered through Continental Kennel Club.
​Genetic Testing:
(all clear)
*Centronuclear Myopathy
*Cystinuria
*Degenerative Myelopathy
*Exercise-induced Collapse
*Myotubular Myopathy 1
*Narcolepsy
*Neonatal Encephalopathy with Seizures
*Progressive Retinal Atrophy
*Progressive Rod Cone
Degeneration
*Retinal Dysplasia/
Oculoskeletal Dysplasia 1
​*Von Willebrand Disease
Hips: OFA Good
Elbows : OFA Normal

Dixie Magnolia's Cajun Gumbeaux

Dixie Magnolia's
Chicory & Cream
'Chicory'
(dam)

​Chicory is an F1bb Third Generation
Small/Medium Size Goldendoodle
She was born on August 11, 2017
She comes from an awesome breeder in Michigan that produces gorgeous, healthy puppies from genetically tested parents.  They have a fabulous hands on program for raising their puppies.
​We are excited to have her join our Dixie Magnolia family 
and are excited to see the beautiful puppies she will produce.
She lives with her Guardian home in Louisiana.

She has a dark apricot non shedding curly fleece coat
and will beapproximately 35 lbs when grown.

Her Mom is a 50 lb. red F1b Goldendoodle
and her Dad is a 55 lb. red standard poodle.

Registered through Continental Kennel Club

Genetic Testing:
(all clear)
*Degenerative Myelopathy
*Ichthyosis (Golden Retriever Type)
*Neonatal Encephalopathy with seizures
*Progressive Retinal Atrophy (Golden Retriever 1)
*Progressive Retinal Atrophy (Golden Retriever 2)
*Progressive Retinal Atrophy,
​ (Progressive Rod Core Degeneratiuon)
*Von Willebrand Disease 1

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​Dixie Magnolia's
​Mint Julep in the Courtyard
'Julep'
​(dam)

​


















​​



​Julep is our F3 Third Generation
​50lb. Small Standard Labradoodle,
born on November 5, 2016

She has a beautiful chocolate colored curly fleece non shedding coat that feels like silk.

Her parents are Gumbeaux and Reaux.

Registered Through Continental Kennel Club

​We are so excited to have her as part of our breeding program and can't wait to see the puppies she will produce in the future.


​ Genetic Testing :
(all clear)
*Centronuclear Myopathy
*Cystinuria
*Degenerative Myelopathy
*Exercise-induced Collapse
*Myotubular Myopathy 1
*Narcolepsy
*Neonatal Encephalopathy with Seizures
*Progressive Retinal Atrophy
*Progressive Rod Cone
Degeneration
*Retinal Dysplasia/
Oculoskeletal Dysplasia 1
​*Von Willebrand Disease

​

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 Dixie Magnolia's King Willoughby
                    'Willoughby'
​                            (sire)

​

• Willoughby is from our 2015 litter between Gumbeaux and Evangeline. (her last litter)
• Willoughby is so exceptional we decided to add him to our breeding program.
  Willoughby is a third generation, F3 Labradoodle. He has a gorgeous silky non shedding chocolate fleece coat with white markings on his chin, chest and toes.
  He is two years old and weighs approximately 60 lbs.
  ​Registered through Continental Kennel Club
  ​Willoughby is super intelligent, affectionate, and loves to go on car rides.
  He loves being a 60 pound 'Lap Dog'!
  
  Genetic Testing:
•  ​(all clear)
  
• *Centronuclear Myopathy
• *Cystinuria
  *Degenerative Myelopathy
  *Exercise-induced Collapse
  *Myotubular Myopathy 1
  *Narcolepsy
  *Neonatal Encephalopathy with Seizures
  *Progressive Retinal Atrophy
  *Progressive Rod Cone
  Degeneration
  *Retinal Dysplasia/
  Oculoskeletal Dysplasia 1
  ​*Von Willebrand Disease​

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Dixie Magnolia's Cajun Creole
"Cajun'
​(sire)

Cajun is a Third Generation chocolate colored medium size Labradoodle from LaReaux and Mardi Gras' Spring 2018 litter.
He has a soft low shedding fleece coat.

​Genetic testing is completed and all clear:
Von Willebrand Disease Type I
Congenital Macrothrombocytopenia
Canine Elliptocytosis
Pyruvate Kinase Deficiency
Progressive Retinal Atrophy - prcd
Progressive rod-cone degeneration (PRCD Exon 1)
Golden Retriever Progressive Retinal Atrophy 2
Progressive Retinal Atrophy - crd4/cord1
AchromatopsiaMacular Corneal Dystrophy (MCD)
Neuronal Ceroid Lipofuscinosis
GM2 Gangliosidosis
Degenerative MyelopathyNeonatal Encephalopathy with Seizures (NEWS)
NarcolepsyMuscular Dystrophy
Centronuclear MyopathyExercise-Induced Collapse
Myotubular Myopathy 1,
X-linked Myotubular Myopathy
Malignant Hyperthermia
Congenital Myasthenic Syndrome
Dystrophic Epidermolysis Bullosa
​MDR1 Drug Sensitivity (MDR1)
P2Y12 Receptor Platelet Disorder (P2RY12)
Factor IX Deficiency, Hemophilia B (F9 Exon 7,​Terrier Variant)
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant)
Factor VII Deficiency (F7 Exon 5)
Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant)
Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1)
Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2)
Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant)
Thrombopathia (RASGRP2 Exon 8)
​Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant)
​Von Willebrand Disease Type II (VWF Exon 28)
​Von Willebrand Disease Type III (VWF Exon 4)
​Von Willebrand Disease Type I (VWF)
​Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3)
​Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant)Canine Elliptocytosis (SPTB Exon 30)
Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20)
​Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12)
May-Hegglin Anomaly (MYH9)
​Prekallikrein Deficiency (KLKB1 Exon 8)
Pyruvate Kinase Deficiency (PKLR Exon 5)
Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant)
Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant)
Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant)
Pyruvate Kinase Deficiency (PKLR Exon 10)
Trapped Neutrophil Syndrome (VPS13B)
Ligneous Membranitis (PLG)
Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant)
Complement 3 (C3) deficiency (C3)
Severe Combined Immunodeficiency (PRKDC)
Severe Combined Immunodeficiency (RAG1)
X-linked Severe Combined Immunodeficiency (IL2RG Variant 1)
X-linked Severe Combined Immunodeficiency (IL2RG Variant 2)
Progressive Retinal Atrophy - rcd1 
Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant)
Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant)
Progressive Retinal Atrophy - rcd3
Rod-cone dysplasia, rcd3 (PDE6A)
Progressive Retinal Atrophy - prcd
Progressive rod-cone degeneration (PRCD Exon 1)
Progressive Retinal Atrophy (CNGB1)Progressive Retinal Atrophy (SAG)
Golden Retriever Progressive Retinal Atrophy 2 (TTC8)
​Progressive Retinal Atrophy - crd1 (PDE6B)
Progressive Retinal Atrophy - crd2 (IQCB1)
Progressive Retinal Atrophy - crd4/cord1 (RPGRIP1)
Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1)
Achromatopsia (CNGA3 Exon 7 German Shepherd Variant)
Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant)Autosomal Dominant Progressive Retinal Atrophy (RHO)
Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2)
Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5)
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion)
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP)
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9)
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17)
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 11)
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant)
Primary Lens Luxation (ADAMTS17)
Congenital stationary night blindness (RPE65)
Macular Corneal Dystrophy (MCD) (CHST6)
2,8-Dihydroxyadenine (2,8-DHA)
Urolithiasis (APRT)
Cystinuria Type I-A (SLC3A1)
Cystinuria Type II-A (SLC3A1)
Cystinuria Type I-A (SLC7A9)
Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9)
Polycystic Kidney Disease (PKD1)
Primary Hyperoxaluria (AGXT)
Protein Losing Nephropathy (NPHS1)
X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35)
Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3)
Primary Ciliary Dyskinesia (CCDC39 Exon 3)
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID) 
Dry Eye Curly Coat Syndrome (FAM83H Exon 5)
X-linked Ectodermal Dysplasia,
Anhidrotic Ectodermal Dysplasia (EDA Intron 8)
Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7)
Glycogen Storage Disease Type II, Pompe's Disease (GAA)
Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC)
Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL)
Mucopolysaccharidosis Type IIIA 
Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1)
Mucopolysaccharidosis Type IIIA
Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2)
Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 5)
Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3)
Glycogen storage disease Type VII
Phosphofructokinase deficiency (PFKM Exon 21)
Glycogen storage disease Type VII
Phosphofructokinase deficiency (PFKM Exon 8)
Lagotto Storage Disease (ATG4D)
Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8)
Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4)
Neuronal Ceroid Lipofuscinosis 1
Cerebellar Ataxia - NCL-A (ARSG Exon 2)
Neuronal Ceroid Lipofuscinosis 1 (CLN5 Exon 4 Variant 1)
Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7)
Neuronal Ceroid Lipofuscinosis 8 (CLN8 Exon 2)
Neuronal Ceroid Lipofuscinosis (MFSD8)Neuronal Ceroid Lipofuscinosis (CLN8)
Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5)Neuronal Ceroid Lipofuscinosis (CLN5 Exon 4 Variant 2)
Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2)
GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant)
GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant)
GM1 Gangliosidosis (GLB1 Exon 2)
GM2 Gangliosidosis (HEXB, Poodle Variant)
GM2 Gangliosidosis (HEXA)
Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5)
Autosomal Recessive Amelogenesis Imperfecta (Italian Greyhound Variant)
Persistent Mullerian Duct Syndrome (AMHR2)
Alaskan Husky Encephalopathy
Subacute Necrotizing Encephalomyelopathy (SLC19A3)
Alexander Disease (GFAP)
Cerebellar Abiotrophy 
Neonatal Cerebellar Cortical Degeneration (SPTBN2)
Cerebellar Ataxia 
Progressive Early-Onset Cerebellar Ataxia (SEL1L)
Cerebellar Hypoplasia (VLDLR)
Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1)
Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10)
Benign Familial Juvenile Epilepsy 
Remitting Focal Epilepsy (LGI2)
Degenerative Myelopathy (SOD1A)
Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2)
Hypomyelination and Tremors (FNIP2)
Shaking Puppy Syndrome,
X-linked Generalized Tremor Syndrome (PLP)
L-2-Hydroxyglutaricaciduria (L2HGDH)
Neonatal Encephalopathy with Seizures (NEWS) (ATF2)
Polyneuropathy, NDRG1 Greyhound Variant (NDRG1
Exon 15)
Polyneuropathy, NDRG1 Malamute Variant (NDRG1
Exon 4)
Narcolepsy (HCRTR2 Intron 6)
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15)
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4)
Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1)
Hereditary Sensory Autonomic Neuropathy (HSAN),
Acral Mutilation Syndrome (GDNF-AS)
Juvenile-Onset Polyneuropathy,
Leonberger Polyneuropathy 1 (LPN1,
ARHGEF10 Dilated Cardiomyopathy (PDK4)
Long QT Syndrome (KCNQ1)
Muscular Dystrophy Cavalier King Charles Spaniel Variant 1
Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )
Muscular Dystrophy
Muscular Dystrophy (DMD Golden Retriever Variant)
Centronuclear Myopathy (PTPLA)
Exercise-Induced Collapse (DNM1)
Inherited Myopathy of Great Danes (BIN1)Myotonia Congenita (CLCN1 Exon 7)
Myotonia Congenita (CLCN1 Exon 23)Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1)
Hypocatalasia, Acatalasemia (CAT)
Pyruvate Dehydrogenase Deficiency (PDP1)
Malignant Hyperthermia (RYR1)
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53)
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8)
Congenital Myasthenic Syndrome (CHAT)
Congenital Myasthenic Syndrome (COLQ)
Episodic Falling Syndrome (BCAN)
Dystrophic Epidermolysis Bullosa (COL7A1)
Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1)
Ichthyosis, Epidermolytic Hyperkeratosis (KRT10)
Ichthyosis (PNPLA1)Ichthyosis (SLC27A4)
Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16)
Hereditary Footpad Hyperkeratosis (FAM83G)
Hereditary Nasal Parakeratosis (SUV39H2)
Musladin-Lueke Syndrome (ADAMTSL2)Cleft Lip and/or Cleft Palate (ADAMTS20)
Hereditary Vitamin D-Resistant Rickets (VDR)
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia (COL9A3, Labrador Retriever)
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2)
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1)
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1)
Osteochondrodysplasia,
​Skeletal Dwarfism (SLC13A1)
Skeletal Dysplasia 2 (COL11A2)
Craniomandibular Osteopathy (CMO) (SLC37A2)

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Dixie Magnolia's Crawfish in the Bayou
'Crawfish'
​(sire)

​



​

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Crawfish is a third generation standard size Double Doodle and comes from our Spring 2018 litter between Beignet and Willoughby.
He hasa a beautiful curly creme colored non shedding coat.
We can't wait to see the puppies he will produce!!

​Genetic testing completed and all clear.
​Von Willebrand Disease Type I
Congenital Macrothrombocytopenia
Canine Elliptocytosis
Pyruvate Kinase Deficiency
Progressive Retinal Atrophy - prcd
Progressive rod-cone degeneration 
Golden Retriever Progressive Retinal Atrophy 2
Progressive Retinal Atrophy - crd4/cord1
Achromatopsia
Macular Corneal Dystrophy 
Neuronal Ceroid Lipofuscinosis
GM2 Gangliosidosis
Degenerative Myelopathy 
Neonatal Encephalopathy with Seizures 
Narcolepsy
Muscular Dystrophy
Muscular Dystrophy (DMD Golden Retriever Variant)
Centronuclear Myopathy
Exercise-Induced Collapse
Myotubular Myopathy 1, X-linked Myotubular Myopathy
Malignant Hyperthermia
Congenital Myasthenic Syndrome
Dystrophic Epidermolysis Bullosa
MDR1 Drug Sensitivity
P2Y12 Receptor Platelet Disorder
Factor IX Deficiency, Hemophilia B 
Factor IX Deficiency, Hemophilia B 
Factor VII Deficiency 
Factor VIII Deficiency, Hemophilia A 
Factor VIII Deficiency, Hemophilia A 
Factor VIII Deficiency, Hemophilia A 
Thrombopathia 
Thrombopathia 
Von Willebrand Disease Type II 
Von Willebrand Disease Type III
Von Willebrand Disease Type 1
Canine Leukocyte Adhesion Deficiency Type III 
Congenital Macrothrombocytopenia 
Canine Elliptocytosis 
Cyclic Neutropenia, Gray Collie Syndrome 
Glanzmann's Thrombasthenia Type I 
May-Hegglin Anomaly 
Prekallikrein Deficiency 
Pyruvate Kinase Deficiency 
Pyruvate Kinase Deficiency 
Pyruvate Kinase Deficiency 
Pyruvate Kinase Deficiency 
Pyruvate Kinase Deficiency 
Trapped Neutrophil Syndrome 
Ligneous Membranitis 
Congenital Hypothyroidism 
Complement 3 
Severe Combined Immunodeficiency 
Severe Combined Immunodeficiency 
X-linked Severe Combined Immunodeficiency 
X-linked Severe Combined Immunodeficiency  2
Progressive Retinal Atrophy - rcd1 Rod-cone dysplasia, rcd1 
Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a 
Progressive Retinal Atrophy - rcd3 Rod-cone dysplasia, rcd3 
Progressive Retinal Atrophy - prcd Progressive rod-cone degeneration 
Progressive Retinal Atrophy 
Progressive Retinal Atrophy 
Golden Retriever Progressive Retinal Atrophy 2 
Progressive Retinal Atrophy - crd1 
Progressive Retinal Atrophy - crd2 
Progressive Retinal Atrophy - crd4/cord1 
Collie Eye Anomaly, Choroidal Hypoplasia 
Achromatopsia 
Autosomal Dominant Progressive Retinol atrophy
Canine Multifocal Retinopathy cmr1 
Canine Multifocal Retinopathy cmr2 
Canine Multifocal Retinopathy cmr3 
Canine Multifocal Retinopathy cmr3  (BEST1 Exon 10 SNP)
Glaucoma Primary Open Angle Glaucoma 
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17)>
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 11)>
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts 
Primary Lens Luxation 
Congenital stationary night blindness 
Macular Corneal Dystrophy 
2,8-Dihydroxyadenine 
Urolithiasis 
Cystinuria Type I-A 
Cystinuria Type II-A 
Cystinuria Type I-A 
Hyperuricosuria and Hyperuricemia or Urolithiasis 
Polycystic Kidney Disease 
Primary Hyperoxaluria 
Protein Losing Nephropathy 
X-Linked Hereditary Nephropathy 
Autosomal Recessive Hereditary Nephropathy,
Familial Nephropathy 
Primary Ciliary Dyskinesia 
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis 
Dry Eye Curly Coat Syndrome 
X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia 
Renal Cystadenocarcinoma and Nodular Dermatofibrosis 
Glycogen Storage Disease Type II, Pompe's Disease 
Glycogen Storage Disease Type Ia, Von Gierke Disease 
Glycogen Storage Disease Type IIIa 
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A 
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A 
Mucopolysaccharidosis Type VII, Sly Syndrome 
Mucopolysaccharidosis Type VII, Sly Syndrome 
Glycogen storage disease Type VII, Phosphofructokinase deficiency 
Glycogen storage disease Type VII, Phosphofructokinase deficiency 
Lagotto Storage Disease 
Neuronal Ceroid Lipofuscinosis 1 
Neuronal Ceroid Lipofuscinosis 2 
Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia - NCL-A 
Neuronal Ceroid Lipofuscinosis 1 
Neuronal Ceroid Lipofuscinosis 6 
Neuronal Ceroid Lipofuscinosis 8 
Neuronal Ceroid Lipofuscinosis (CLN8)
Neuronal Ceroid Lipofuscinosis (MFSD8)
Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5)
Neuronal Ceroid Lipofuscinosis (CLN5 Exon 4 Variant 2)
Adult-Onset Neuronal Ceroid Lipofuscinosis 
GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Varient)
GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant)>
GM1 Gangliosidosis (GLB1 Exon 2)
GM2 Gangliosidosis (HEXB, Poodle Variant)
GM2 Gangliosidosis (HEXA)
Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5)
Autosomal Recessive Amelogenesis Imperfecta (Italian Greyhound Variant)
Persistent Mullerian Duct Syndrome (AMHR2)
Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3)
Alexander Disease (GFAP)
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration 
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia 
Cerebellar Hypoplasia 
Spinocerebellar Ataxia, Late-Onset Ataxia 
Spinocerebellar Ataxia with Myokymia and/or Seizures 
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy 
Degenerative Myelopathy 
Fetal-Onset Neonatal Neuroaxonal Dystrophy 
Hypomyelination and Tremors 
Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome 
L-2-Hydroxyglutaricaciduria 
Neonatal Encephalopathy with Seizures 
Polyneuropathy, NDRG1 Greyhound Variant 
Polyneuropathy, NDRG1 Malamute Variant 
Narcolepsy 
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) 
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) 
Juvenile Laryngeal Paralysis and Polyneuropathy 
Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS)>
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 
Dilated Cardiomyopathy 
Long QT Syndrome (KCNQ1)
Muscular Dystrophy Cavalier King Charles Spaniel Variant 1
Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )
Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant)
Centronuclear Myopathy (PTPLA)
Exercise-Induced Collapse (DNM1)
Inherited Myopathy of Great Danes (BIN1)
Myotonia Congenita (CLCN1 Exon 7)
Myotonia Congenita (CLCN1 Exon 23)
Myotubular Myopathy 1, X-linked Myotubular Myopathy
Hypocatalasia, Acatalasemia (CAT)
Pyruvate Dehydrogenase Deficiency (PDP1)
Malignant Hyperthermia (RYR1)
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53)
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8)
Congenital Myasthenic Syndrome (CHAT)>
Congenital Myasthenic Syndrome (COLQ)>
Episodic Falling Syndrome (BCAN)
Dystrophic Epidermolysis Bullosa (COL7A1)>
Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1)>
Ichthyosis, Epidermolytic Hyperkeratosis (KRT10)>
Ichthyosis (PNPLA1)>
Ichthyosis (SLC27A4)>
Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16)>
Hereditary Footpad Hyperkeratosis (FAM83G)>
Hereditary Nasal Parakeratosis (SUV39H2)>
Musladin-Lueke Syndrome (ADAMTSL2)
Cleft Lip and/or Cleft Palate (ADAMTS20)
Hereditary Vitamin D-Resistant Rickets (VDR)>
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia (COL9A3, Labrador Retriever)>
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2)>
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1)>
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1)>
Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1)>
Skeletal Dysplasia 2 (COL11A2)>
Craniomandibular Osteopathy (CMO) (SLC37A2)>
​

Retired
Magnolia Belle Evangeline Jolie
(Angie)
​Angie is now retired at age 6. She gave us four beautiful litter​​s of F1b Labradoodle puppies who have all gone on to live fabulous lives with their new families.  Angie was the best mother you could ever ask for. She was the 'perfect' Mom.  She tirelessly cared for her pups,  keeping them spotless and well fed,  and guarded them with her life. Three of her puppies, Reaux, Julep and Willoughby (above) will
​carry on her legacy.