Bonnie
Bonnie is our cream F3 multi generation Miniature Goldendoodle girl. She is 17 inches to the shoulder and weighs around 14kg. Bonnie’s mother is a standard Goldendoodle named Sukey and her father is a miniature Poodle named Bailey. We are very familiar with Bonnie’s family history as she was seen with her mother Sukey and grandmother Betty and we also own Bonnie’s half brother Bruno from a previous litter.
Bonnie is the most well attentive and loyal dog with such a gentle, sweet and loving nature and is full of character. Bonnie has always been super easy to train, was quick to learn and is always eager to please. She has successfully taken part in gun dog classes to engage her intelligent mind and gets a lot of admirers wherever she goes for her pretty looks with her beautifully soft and wavy non shedding coat, her exceptional recall and her wonderful temperament being the affectionate and obedient dog that she is. These are all really important traits that she will pass onto her puppies. She loves nothing more than chasing balls and sticks and going for long walks and runs through the fields. Bonnie is such an amazing girl who really makes us so proud every day.
Bonnie is proving to be a such a wonderful mother to her babies. It is an absolute joy to watch her nurture them so beautifully and we look forward to seeing them all blossom into well rounded puppies! Both Bonnie and Bertie have all the best attributes of the breed that will be passed down to their puppies.
Bonnie is fully DNA health tested with clear results for all hereditary diseases found in this breed meaning her puppies will not be affected by any of these horrible diseases. The main ones are listed below:
Degenerative Myelopathy SOD1 (c.100G>A) CLEAR
Dystrophic Epidermolysis Bullosa COL7A1 (c.5716G>A) CLEAR
Gangliosidosis GM2 HEXB (c.283delG) CLEAR
Golden Retriever PRA1 SLC4A3 (c.2601_2602insC) CLEAR
Ichthyosis (Golden Retriever) PNPLA1 (c.1445_1447delACCinsTACTACTA) CLEAR
Muscular Dystrophy DMD () CLEAR
Neonatal Encephalopathy with Seizures ATF2 (c.152T>G) CLEAR
Osteochondrodysplasia SLC13A1 () CLEAR
Osteogenesis Imperfecta COL1A1 (c.1276G>C) CLEAR
Progressive Retinal Atrophy (GR-PRA2) TTC8 (c.669delA) CLEAR
Progressive Retinal Atrophy (PRA-PRCD) PRCD (c.5G>A) CLEAR
Sensory Ataxic Neuropathy tRNA-Tyr (m.5305delA) CLEAR
Von Willebrand Disease I VWF (c.7437G>A) CLEAR