Pedigree database Golden Retriever » BRIERFORD FIONN OF GREENGLEN

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Nick: BRIERFORD FIONN OF GREENGLEN Date of birth: 00/00/1964 Sex Male Place of birth:   --- Kennel (Breeder): Breeder: Mrs Harrison Living place :   --- City: Kennel (Owner): Owner: Rev. R. Hutchison Father: CAMROSE TALLYRAND OF ANBRIA Mother: BOLTBY FELICITY OF BRIERFORD Bonitation code: Character test: Training: Tatoo: Organization: Pedigree number: Chip: Titles:

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Pedigree analysis

Generations: 3  4  5  6  7  8  9  10    Pedigree code

CAMROSE TALLYRAND OF ANBRIA     1960-04-20 CAMROSE FANTANGO     1951-11-11 DORCAS TIMBERSCOMBE TOPPER     1946-05-17 DORCAS BRUIN      TIMBERSCOMBE TREFOIL      GOLDEN CAMROSE TESS     1946-00-00 SHERRYDAN DAMSON      SUNSHINE OF SLAT      JANE OF ANBRIA     1952-06-30 WILLIAM OF WESTLEY     1947-01-11 SPAR OF YELME      SUSAN OF WESTLEY      BRIAR OF ARBROOK      DORCAS GLORIOUS OF SLAT      HEATHERBELLE OF ARBROOK      BOLTBY FELICITY OF BRIERFORD     1962-11-22 CABUS CADET     1959-12-01 BEAUCHASSE JASON      SOLWAY LADDIE      BEAUCHASSE IMPRINT     1953-08-13 BRECKLANDS TAMARIS     1956-06-01 BRECKLANDS REPORTER      BRECKLANDS SHANI OF BREYDONVALE      BOLTBY SUGAR BUSH     1956-04-14 BOLTBY SKYLON     1951-07-03 BOLTBY KYMBA     1948-05-22 BOLTBY SWEET MELODY      BOLTBY GILLRAIN GALALINDA      BOLTBY MOONRAKER     1949-12-26 GILLRAIN SUSAN     1951-03-30

Offsprings:  FAIRWOOD'S DUCK APORTER      WHITEWATER JANE      WHITEWATER JO

Siblings:

Breedings:  LINDYS ORIANA      SALLY OF WHITEWATER

Patellar luxation	PL
Hip dysplasia	HD
Elbow dysplasia	ED
Progressive Retinal Degeneration	PRA
Bite	Прикус
Primary Сiliагу Dyskinesia	PCD
Brainstem Auditory Evoked Response	BAER
Multi-Drug Resistance 1	MDR1
Thyroid	THYROID
Copper Toxicosis	CT
Degenerative Myelopathy	DM
Mucopolysaccharidosis	MPS
Primary Lens Luxation	PLL
Coat Length	CL
Entlebucher Urinary Syndrome	EUS
Cystinuria	Cystinuria
Musladin-Leuke Syndrome	MLS
Factor VII	Factor VII
Neonatal Cerebellar Cortical Degeneration	NCCD
Imerslund-Grasbeck syndrome	IGS
von Willebrand disease	vWD
Dwarfism	DW
Exercise-induced collapse	EIC
Hereditary nasal parakeratosis	HNPK

Notes: 

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