Mabry Labradors Located in Murphysboro IL

​Chicago

CHOCOLATE LABS FOR SALE

Healthy Paws Pet Insurance and Foundation.

We are located in Murphysboro IL. 

AKC CHOCOLATE LABS

Mabry Labs
flat fee listing

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We currently have  two open chocolate male puppies at this time.


Please, see future litter page for upcoming litters.

Updated: 10/13/2019


Babe and Moe had a litter on 8/6/2019
The following are open puppies in the litter.

Chocolate male second pick
Chocolate male third pick

Puppies in this litter are $1800.00 Limited AKC ask about Full AKC
Deposit of $300.00 is required to reserve a puppy.
Balance of $1500 is due before the puppy is released to go home. 

Contact Wendy Mabry at mabrywendy@gmail.com or call/text 618-521-5719

You can place a deposit to hold on of the chocolate males by using this link.






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These pups are guaranteed to not be affected by the following:


  • Coagulation factor VII deficiency
  • Elliptocytosis
  • Leukocyte adhesion deficiency, type III
  • May-Hegglin anomaly
  • P2RY12 receptor platelet disorder
  • Prekallikrein deficiency
  • Pyruvate kinase deficiency
  • Von Willebrand disease
  • Renal cystadenocarcinoma and nodular dermatofibrosis
  • Amelogenesis imperfecta
  • Multidrug resistance 1
  • Cone degeneration
  • Congenital stationary night blindness
  • Dry eye curly coat syndrome
  • Early retinal degeneration
  • Hereditary cataracts
  • Juvenile Laryngeal Paralysis and Polyneuropathy
  • Multifocal retinopathy 1
  • Multifocal retinopathy 2
  • Multifocal retinopathy 3
  • Primary lens luxation
  • Primary open angle glaucoma
  • Progressive retinal atrophy, Cone-rod dystrophy
  • Progressive retinal atrophy
  • Progressive rod-cone degeneration
  • Progressive retinal atrophy Rod-cone dysplasia 3
  • Progressive retinal atrophy, generalized
  • Complement 3 deficiency
  • Primary ciliary dyskinesia
  • Trapped neutrophil syndrome
  • Gallbladder mucoceles
  • Glycogen storage disease IIIa
  • Adult-onset neuronal ceroid lipofuscinosis
  • Glycogen storage disease IIIa
  • Glycogen storage disease Ia
  • Glycogen storage disease VII
  • Mucopolysaccharidosis I
  • Neuronal ceroid lipofuscinosis 1
  • Neuronal ceroid lipofuscinosis 10
  • Neuronal ceroid lipofuscinosis 2
  • Neuronal ceroid lipofuscinosis 4A
  • Neuronal ceroid lipofuscinosis 5
  • Neuronal ceroid lipofuscinosis 6
  • Pompe disease
  • Pyruvate dehydrogenase deficiency
  • Pyruvate kinase deficiency
  • Juvenile Laryngeal Paralysis and Polyneuropathy
  • Adult-onset neuronal ceroid lipofuscinosis
  • Congenital myasthenic syndrome
  • Degenerative myelopathy
  • Exercise-induced collapse
  • Glycogen storage disease IIIa
  • Juvenile Laryngeal Paralysis and Polyneuropathy
  • Mucopolysaccharidosis I
  • Musladin-Lueke syndrome
  • Myotubular myopathy 1
  • Osteochondrodysplasia
  • Pompe disease
  • Skeletal dysplasia 2
  • Adult-onset neuronal ceroid lipofuscinosis
  • Benign familial juvenile epilepsy
  • Congenital myasthenic syndrome
  • Degenerative myelopathy
  • Episodic falling syndrome
  • Exercise-induced collapse
  • Juvenile Laryngeal Paralysis and Polyneuropathy
  • Late onset ataxia
  • Mucopolysaccharidosis I
  • Musladin-Lueke syndrome
  • Narcolepsy
  • Neonatal cerebellar cortical degeneration
  • Neonatal encephalopathy with seizures
  • Neuronal ceroid lipofuscinosis 1
  • Neuronal ceroid lipofuscinosis 10
  • Neuronal ceroid lipofuscinosis 2
  • Neuronal ceroid lipofuscinosis 4A
  • Neuronal ceroid lipofuscinosis 5
  • Neuronal ceroid lipofuscinosis 6
  • Sensory ataxic neuropathy
  • Spinocerebellar ataxia
  • Startle disease
  • Primary ciliary dyskinesia
  • Primary ciliary dyskinesia
  • Anhidrotic ectodermal dysplasia
  • Dry eye curly coat syndrome
  • Dystrophic epidermolysis bullosa
  • Ectodermal dysplasia
  • Epidermolytic hyperkeratosis
  • Hereditary nasal parakeratosis
  • Renal cystadenocarcinoma and nodular dermatofibrosis
  • Fanconi syndrome
  • Hyperuricosuria
  • Persistent Müllerian duct syndrome
  • Primary ciliary dyskinesia
  • Primary hyperoxaluria
  • Renal cystadenocarcinoma and nodular dermatofibrosis





  • Puppies come with the following:


    AKC papers
    Vaccinations, we give vaccines weeks, 4, 6 and 8.
    De-wormed from day three until they leave. 11 intestinal worms (including roundworm, whipworm, hookworm, tapeworm and hydatid tapeworm)
    Given prevention medication for Giardia and Coccdia
    Pet insurance for 30 days included for free, pays out 90% of bill with a $250 deductible starting the moment you leave with your puppy. This is a new insurance beginning January 2019.
    One year congenital guarantee
    36-month  guarantee
    EIC, CNM,PRA, PKD, DM, HU, DILUTE, RD/OSD, AND HNPK unaffected
    Socialized
    Access to water for swimming when weather allows. 
    Microchip with no fee
    Puppy food, collar, blanket, reusable tote, microchip, shampoo,  leash, treats, toys, puppy information packet
    Basic commands started such as sitting to wait on food and treats.
    City sounds, fireworks sounds and thunderstorm sounds are started from two weeks old.
    Introduced to other animals and people.
    Puppy culture from day one
    Housebreaking started prior to leaving.
    We are here to answer any questions before and after the sale of the puppy for life of the puppy. Pedigrees of parents  will be provided. 
    All AKC registration papers will be handed over at the time of puppy pick up.
    Thank you for looking at our website and we hope to see you soon for your next labrador puppy. We can guarantee that in Illinois we do the most work for our adults and puppies. No other breeder comes close to do all this. We have some attempting to copy us, but if you go to their kennel you will see not one is a real kennel like ours. Garages, basements, living rooms, bedrooms are not a real kennel and those breeders that have bred more than five years with multiple litters should invest the money into a kennel to house their adults better than dog houses or back rooms! lab puppy, lab puppies for sale, akc lab puppies for sale.




    THREE YEAR HIP GUARANTEE AND A ONE YEAR CONGENITAL HEALTH GUARANTEE!







  • Coagulation factor VII deficiency
  • Elliptocytosis
  • Leukocyte adhesion deficiency, type III
  • May-Hegglin anomaly
  • P2RY12 receptor platelet disorder
  • Prekallikrein deficiency
  • Pyruvate kinase deficiency
  • Von Willebrand disease
  • Renal cystadenocarcinoma and nodular dermatofibrosis
  • Amelogenesis imperfecta
  • Multidrug resistance 1
  • Cone degeneration
  • Congenital stationary night blindness
  • Dry eye curly coat syndrome
  • Early retinal degeneration
  • Hereditary cataracts
  • Juvenile Laryngeal Paralysis and Polyneuropathy
  • Multifocal retinopathy 1
  • Multifocal retinopathy 2
  • Multifocal retinopathy 3
  • Primary lens luxation
  • Primary open angle glaucoma
  • Progressive retinal atrophy, Cone-rod dystrophy
  • Progressive retinal atrophy
  • Progressive rod-cone degeneration
  • Progressive retinal atrophy Rod-cone dysplasia 3
  • Progressive retinal atrophy, generalized
  • Complement 3 deficiency
  • Primary ciliary dyskinesia
  • Trapped neutrophil syndrome
  • Gallbladder mucoceles
  • Glycogen storage disease IIIa
  • Adult-onset neuronal ceroid lipofuscinosis
  • Glycogen storage disease IIIa
  • Glycogen storage disease Ia
  • Glycogen storage disease VII
  • Mucopolysaccharidosis I
  • Neuronal ceroid lipofuscinosis 1
  • Neuronal ceroid lipofuscinosis 10
  • Neuronal ceroid lipofuscinosis 2
  • Neuronal ceroid lipofuscinosis 4A
  • Neuronal ceroid lipofuscinosis 5
  • Neuronal ceroid lipofuscinosis 6
  • Pompe disease
  • Pyruvate dehydrogenase deficiency
  • Pyruvate kinase deficiency
  • Juvenile Laryngeal Paralysis and Polyneuropathy
  • Adult-onset neuronal ceroid lipofuscinosis
  • Congenital myasthenic syndrome
  • Degenerative myelopathy
  • Exercise-induced collapse
  • Glycogen storage disease IIIa
  • Juvenile Laryngeal Paralysis and Polyneuropathy
  • Mucopolysaccharidosis I
  • Musladin-Lueke syndrome
  • Myotubular myopathy 1
  • Osteochondrodysplasia
  • Pompe disease
  • Skeletal dysplasia 2
  • Adult-onset neuronal ceroid lipofuscinosis
  • Benign familial juvenile epilepsy
  • Congenital myasthenic syndrome
  • Degenerative myelopathy
  • Episodic falling syndrome
  • Exercise-induced collapse
  • Juvenile Laryngeal Paralysis and Polyneuropathy
  • Late onset ataxia
  • Mucopolysaccharidosis I
  • Musladin-Lueke syndrome
  • Narcolepsy
  • Neonatal cerebellar cortical degeneration
  • Neonatal encephalopathy with seizures
  • Neuronal ceroid lipofuscinosis 1
  • Neuronal ceroid lipofuscinosis 10
  • Neuronal ceroid lipofuscinosis 2
  • Neuronal ceroid lipofuscinosis 4A
  • Neuronal ceroid lipofuscinosis 5
  • Neuronal ceroid lipofuscinosis 6
  • Sensory ataxic neuropathy
  • Spinocerebellar ataxia
  • Startle disease
  • Primary ciliary dyskinesia
  • Primary ciliary dyskinesia
  • Anhidrotic ectodermal dysplasia
  • Dry eye curly coat syndrome
  • Dystrophic epidermolysis bullosa
  • Ectodermal dysplasia
  • Epidermolytic hyperkeratosis
  • Hereditary nasal parakeratosis
  • Renal cystadenocarcinoma and nodular dermatofibrosis
  • Fanconi syndrome
  • Hyperuricosuria
  • Persistent Müllerian duct syndrome
  • Primary ciliary dyskinesia
  • Primary hyperoxaluria
  • Renal cystadenocarcinoma and nodular dermatofibrosis