Darby's Grandpa - Yukon

Darby & Doogie

Large Mini Goldendoodles

Around 40lbs at Maturity

Puppies will be Ready October 12th

$2500 Solid Colors

$3000 With White Markings

ONE PUPPY AVAILABLE

THESE PUPPIES WILL NOT BE AFFECTED BY OVER 160 DIFFERENT GENETICALLY BASED DNA HEALTH ISSUES!

Including: Clinical Genetic Issues, Blood, Hormones, Immune

Issues, Eyes, Kidney, Bladder, Multisystem Issues, Brain & Spinal Cord/Neurological, Heart, Muscular Issues, Metabolic Issues, Gastrointestinal, Neuromuscular, Skin & Connective Tissues,

Skeletal Issues

DAISY

This puppy was not picked today - and is available to a loving home now. She is PERFECT! She has a gorgeous non-shed coat that would be perfect for allergy concerns. Her disposition is very calm but playful. She is a fun puppy that is not a barker, she is submissive and sweet natured and adores everyone. She is litter box trained as well. She is from health tested parents and she cannot ever be affected by over 150 different DNA tested genetic health issues. IF YOU WOULD LIKE TO MEET HER - YOU CAN COME IN PERSON OR SET UP A SKYPE APPOINTMENT. She can be delivered to Albany or Syracuse on Monday or SHE CAN GO FOR 2 WEEKS OF PUPPY SCHOOL. You can call or text 585-623-0426 for more information

DEPOSIT LIST:

These puppy picking days and times cannot be changed. You can come in person or we will help you choose using SKYPE. BE SURE TO GO THROUGH ALL 4 OF THE CUSTOMER INFO SECTIONS (access this by clicking on the tab at the top of any page) INCLUDING THE PUPPY PAPERWORK VIDEO... BEFORE COMING TO YOUR PICKING APPOINTMENT! This way you will have more time to play with the puppies and choose your new baby!

1. LAKESHORE DOODLES - TROBE: GUARDIAN HOME 
    Puppy picking appointment: October 12 at 9 am - IF WE CHOOSE TO KEEP HER
2. Acciari - Dep Rcvd
    Puppy picking appointment: October 12 at 10 am
3. Tol Ho - Dep Rcvd
    Puppy picking appointment: October 12 at 11 am
4. DeFrutos - Dep Rcvd
    Puppy picking appointment: October 12 at 12 pm
5. Gallipoli - Skype - Dep Rcvd
    Puppy picking appointment: October 12 at 1pm
6. Lowenstein - In person - dep rcvd
    Puppy picking appointment: October 12 at 2 pm
7. Cullinane
    Puppy picking appointment: October 12 at 3 pm
8. Limbach Skype - Dep Rcvd
    Puppy picking appointment: October 12 at 4 pm
9. AVAILABLE
    Puppy picking appointment: October 12 at 5 pm
 

Litter Information:

Darby & Doogie Health Tested Lines    $3000

Date of Birth: August 14, 2019

Medium Multigen Goldendoodles                               

Around 40 lbs at Maturity

Go Home Date: October 12, 2019  

Darby - 59 lbs & 22.5"
Doogie - 26lbs and 17"

F1b Goldendoodle x F2b Goldendoodle

Coat Types Expected: Wavey, Loose Curl & Curl

Coat Colors: Cream, Red, Apricot, Gold, Parti Color, Some w/white

Now Taking $100 Deposits

DARBY: F1b Standard Goldendoodle: Hips, Elbows, Patella, Heart

Darby's Dad: Niko Standard Poodle

Hips, Elbows, Patella, Heart

Niko's Dad: Deg Myelopathy, NE, VWD, Macrothrombocytopenia

Darby's Mom: F1 Goldendoodle: Hips elbows, patella, Heart

Darby's Grandma: Kenzie Vazzana Hips

Darby's Grandfather Yukon Eng Golden  Hip, elbow, heart, patella

Darby's Grandfather- Yukon

Darby's Father- Niko

DOOGIE

F2B ENGLISH MINI GOLDENDOODLE

DOOGIE's Health Clearances: 

  • Hips​ - Clear

  • Elbows - Clear

  • Patella - Clear

  • Heart - Clear

  • Von Willebrand Disease Type 1 - Clear

  • Congenital Macrothrombocytopenia - Clear

  • Progressive Retinal Atrophy - prcd 

       Progressive rod-cone degeneration ​- Clear

  • Golden Retriever Progressive Retinal Atrophy 2 - Clear

  • Neuronal Ceroid Lipofuscinosis - Clear

  • GM2 Gangliosidosis - Clear

  • Degenerative Myelopathy - Clear

  • Neonatal Encephalopathy with Seizures - Clear

  • Muscular Dystrophy - Clear

  • Malignant Hyperthermia - Clear

  • Dystrophic Epidermolysis Bullosa - Clear

  • Ichthyosis - Clear

  • Osteogenesis Imperfecta, Brittle Bone Disease - Clear

  • Osteochondrodysplasia Skeletal Dwarfism - Clear

DOOGIE IS ALSO CLEAR ON 145

ADDITIONAL GENETIC TESTS:

Doogie tested CLEAR for all these conditions:

  • MDR1 Drug Sensitivity (MDR1) (Chromosome 14)

  • P2Y12 Receptor Platelet Disorder (P2RY12) (Chromosome 23)

  • Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant) (Chromosome X)

  • Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant) (Chromosome X)

  • Factor VII Deficiency (F7 Exon 5) (Chromosome 22)

  • Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant) (Chromosome X)

  • Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1) (Chromosome X)

  • Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2) (Chromosome X)

  • Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant) (Chromosome 18)

  • Thrombopathia (RASGRP2 Exon 8) (Chromosome 18)

  • Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant) (Chromosome 18)

  • Von Willebrand Disease Type II (VWF Exon 28) (Chromosome 27)

  • Von Willebrand Disease Type III (VWF Exon 4) (Chromosome 27)

  • Von Willebrand Disease Type I (VWF) (Chromosome 27)

  • Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3) (Chromosome 18)

  • Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant) (Chromosome 24)

  • Canine Elliptocytosis (SPTB Exon 30) (Chromosome 8)

  • Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20) (Chromosome 31)

  • Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12) (Chromosome 9)

  • May-Hegglin Anomaly (MYH9) (Chromosome 10)

  • Prekallikrein Deficiency (KLKB1 Exon 8) (Chromosome 16)

  • Pyruvate Kinase Deficiency (PKLR Exon 5) (Chromosome 7)

  • Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant) (Chromosome 7)

  • Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant) (Chromosome 7)

  • Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant) (Chromosome 7)

  • Pyruvate Kinase Deficiency (PKLR Exon 10) (Chromosome 7)

  • Trapped Neutrophil Syndrome (VPS13B) (Chromosome 13)

  • Ligneous Membranitis (PLG) (Chromosome 1)

  • Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant) (Chromosome 17)

  • Complement 3 (C3) deficiency (C3) (Chromosome 20)

  • Severe Combined Immunodeficiency (PRKDC) (Chromosome 29)

  • Severe Combined Immunodeficiency (RAG1) (Chromosome 18)

  • X-linked Severe Combined Immunodeficiency (IL2RG Variant 1) (Chromosome X)

  • X-linked Severe Combined Immunodeficiency (IL2RG Variant 2) (Chromosome X)

  • Progressive Retinal Atrophy - rcd1 Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant) (Chromosome 3)

  • Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant) (Chromosome 3)

  • Progressive Retinal Atrophy - rcd3 Rod-cone dysplasia, rcd3 (PDE6A) (Chromosome 4)

  • Progressive Retinal Atrophy - CNGA (CNGA1 Exon 9) (Chromosome 13)

  • Progressive Retinal Atrophy - prcd Progressive rod-cone degeneration (PRCD Exon 1) (Chromosome 9)

  • Progressive Retinal Atrophy (CNGB1) (Chromosome 2)

  • Progressive Retinal Atrophy (SAG) (Chromosome 25)

  • Golden Retriever Progressive Retinal Atrophy 2 (TTC8) (Chromosome 8)

  • Progressive Retinal Atrophy - crd1 (PDE6B) (Chromosome 3)

  • Progressive Retinal Atrophy - crd2 (IQCB1) (Chromosome 33)

  • Progressive Retinal Atrophy - crd4/cord1 (RPGRIP1) (Chromosome 15)

  • Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1) (Chromosome 37)

  • Achromatopsia (CNGA3 Exon 7 German Shepherd Variant) (Chromosome 10)

  • Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant) (Chromosome 10)

  • Autosomal Dominant Progressive Retinal Atrophy (RHO) (Chromosome 20)

  • Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2) (Chromosome 18)

  • Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5) (Chromosome 18)

  • Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion) (Chromosome 18)

  • Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP) (Chromosome 18)

  • Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9) (Chromosome 20)

  • Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17) (Chromosome 20)

  • Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 12) (Chromosome 3)

  • Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Boston Terrier Variant) (Chromosome 5)

  • Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant) (Chromosome 5)

  • Primary Lens Luxation (ADAMTS17) (Chromosome 3)

  • Congenital stationary night blindness (RPE65) (Chromosome 6)

  • Macular Corneal Dystrophy (MCD) (CHST6) (Chromosome 5)

  • 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis (APRT) (Chromosome 5)

  • Cystinuria Type I-A (SLC3A1) (Chromosome 10)

  • Cystinuria Type II-A (SLC3A1) (Chromosome 10)

  • Cystinuria Type I-A (SLC7A9) (Chromosome 1)

  • Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9) (Chromosome 3)

  • Polycystic Kidney Disease (PKD1) (Chromosome 6)

  • Primary Hyperoxaluria (AGXT) (Chromosome 25)

  • Protein Losing Nephropathy (NPHS1) (Chromosome 1)

  • X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35) (Chromosome X)

  • Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3) (Chromosome 25)

  • Primary Ciliary Dyskinesia (CCDC39 Exon 3) (Chromosome 34)

  • Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5) (Chromosome 13)

  • X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8) (Chromosome X)

  • Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7) (Chromosome 5)

  • Glycogen Storage Disease Type II, Pompe's Disease (GAA) (Chromosome 9)

  • Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC) (Chromosome 9)

  • Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL) (Chromosome 6)

  • Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1) (Chromosome 9)

  • Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2) (Chromosome 9)

  • Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 5) (Chromosome 6)

  • Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3) (Chromosome 6)

  • Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 21) (Chromosome 27)

  • Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 8) (Chromosome 27)

  • Lagotto Storage Disease (ATG4D) (Chromosome 20)

  • Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8) (Chromosome 15)

  • Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4) (Chromosome 21)

  • Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia - NCL-A (ARSG Exon 2) (Chromosome 9)

  • Neuronal Ceroid Lipofuscinosis 1 (CLN5 Exon 4 Variant 1) (Chromosome 22)

  • Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7) (Chromosome 30)

  • Neuronal Ceroid Lipofuscinosis 8 (CLN8 Exon 2) (Chromosome 37)

  • Neuronal Ceroid Lipofuscinosis (MFSD8) (Chromosome 19)

  • Neuronal Ceroid Lipofuscinosis (CLN8) (Chromosome 37)

  • Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5) (Chromosome 18)

  • Neuronal Ceroid Lipofuscinosis (CLN5 Exon 4 Variant 2) (Chromosome 22)

  • Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2) (Chromosome 2)

  • GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant) (Chromosome 23)

  • GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant) (Chromosome 23)

  • GM1 Gangliosidosis (GLB1 Exon 2) (Chromosome 23)

  • GM2 Gangliosidosis (HEXB, Poodle Variant) (Chromosome 2)

  • GM2 Gangliosidosis (HEXA) (Chromosome 30)

  • Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5) (Chromosome 8)

  • Autosomal Recessive Amelogenesis Imperfecta (Italian Greyhound Variant) (Chromosome 13)

  • Persistent Mullerian Duct Syndrome (AMHR2) (Chromosome 27)

  • Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3) (Chromosome 25)

  • Alexander Disease (GFAP) (Chromosome 9)

  • Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2) (Chromosome 18)

  • Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L) (Chromosome 8)

  • Cerebellar Hypoplasia (VLDLR) (Chromosome 1)

  • Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1) (Chromosome 18)

  • Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10) (Chromosome 38)

  • Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2) (Chromosome 3)

  • Degenerative Myelopathy (SOD1A) (Chromosome 31)

  • Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2) (Chromosome 2)

  • Hypomyelination and Tremors (FNIP2) (Chromosome 15)

  • Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP) (Chromosome X)

  • L-2-Hydroxyglutaricaciduria (L2HGDH) (Chromosome 0)

  • Neonatal Encephalopathy with Seizures (NEWS) (ATF2) (Chromosome 36)

  • Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15) (Chromosome 13)

  • Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4) (Chromosome 13)

  • Narcolepsy (HCRTR2 Intron 6) (Chromosome 12)

  • Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15) (Chromosome 1)

  • Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4) (Chromosome 1)

  • Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1) (Chromosome 19)

  • Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS) (Chromosome 4)

  • Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10) (Chromosome 16)

  • Dilated Cardiomyopathy (PDK4) (Chromosome 14)

  • Long QT Syndrome (KCNQ1) (Chromosome 18)

  • Muscular Dystrophy Cavalier King Charles Spaniel Variant 1 (Chromosome X)

  • Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant ) (Chromosome X)

  • Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant) (Chromosome X)

  • Centronuclear Myopathy (PTPLA) (Chromosome 2)

  • Exercise-Induced Collapse (DNM1) (Chromosome 9)

  • Inherited Myopathy of Great Danes (BIN1) (Chromosome 19)

  • Myotonia Congenita (CLCN1 Exon 7) (Chromosome 16)

  • Myotonia Congenita (CLCN1 Exon 23) (Chromosome 16)

  • Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1) (Chromosome X)

  • Hypocatalasia, Acatalasemia (CAT) (Chromosome 18)

  • Pyruvate Dehydrogenase Deficiency (PDP1) (Chromosome 29)

  • Malignant Hyperthermia (RYR1) (Chromosome 1)

  • Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53) (Chromosome 2)

  • Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8) (Chromosome 2)

  • Congenital Myasthenic Syndrome (CHAT) (Chromosome 28)

  • Congenital Myasthenic Syndrome (COLQ) (Chromosome 23)

  • Episodic Falling Syndrome (BCAN) (Chromosome 7)

  • Dystrophic Epidermolysis Bullosa (COL7A1) (Chromosome 20)

  • Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1) (Chromosome 7)

  • Ichthyosis, Epidermolytic Hyperkeratosis (KRT10) (Chromosome 9)

  • Ichthyosis (PNPLA1) (Chromosome 12)

  • Ichthyosis (SLC27A4) (Chromosome 9)

  • Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16) (Chromosome 9)

  • Hereditary Footpad Hyperkeratosis (FAM83G) (Chromosome 5)

  • Hereditary Nasal Parakeratosis (SUV39H2) (Chromosome 2)

  • Musladin-Lueke Syndrome (ADAMTSL2) (Chromosome 9)

  • Cleft Lip and/or Cleft Palate (ADAMTS20) (Chromosome 27)

  • Hereditary Vitamin D-Resistant Rickets (VDR) (Chromosome 27)

  • Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia (COL9A3, Labrador Retriever) (Chromosome 24)

  • Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) (Chromosome 14)

  • Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1) (Chromosome 21)

  • Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) (Chromosome 9)

  • Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1) (Chromosome 14)

  • Skeletal Dysplasia 2 (COL11A2) (Chromosome 12)

  • Craniomandibular Osteopathy (CMO) (SLC37A2) (Chromosome 5)

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Call or Text (585) 623-0426

NYS PD #365