Black Lab puppies for sale

The black female is guaranteed to not be affected by any of 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
  • 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

    • Black lab puppies for sale

    Black Lab Puppies For Sale

    ​​

     


    The black lab puppies we have range in size and type. We have them small under 50 pounds and over 100 pounds.  Please, if you have a size requirement make sure to look at our litter lists to see what sizes are expected in the litters. We only estimate sizes we can not guarantee them, however we a generally within 20% of the adult weight range we predict. There are a lot of factors that go into adult size that we will discuss with you if you need.


    Please, send an email to mabrywendy@gmail.com for information on any black lab puppy you are interested in. 



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    lab puppies for sale

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    UPDATED 10/13/2019


    We have one black female at this time. 


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

    Black female 
    Puppies in this litter are $1800.00 
    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 on this puppy  by using this link.



    Black lab puppies for sale

    Mabry Labradors Located in Murphysboro IL

    ​Chicago

    We are located in Murphysboro IL. 

    Mabry Labs
    Healthy Paws Pet Insurance and Foundation.
    flat fee listing