Genetic study of Welsh gypsies.
Open Access
- 1 June 1977
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 14 (3) , 172-176
- https://doi.org/10.1136/jmg.14.3.172
Abstract
A South Wales gypsy kindred of Romany origin had a high incidence of phenylketonuria along with other recessively inherited disorders. There was a high degree of consanguinity (F = 0-017) with an excess of non-specific mental subnormality among known consanguineous matings. Phenylketonuria and a number of other recessively inherited disorders have been recorded from other Romany gypsy populations, but it is uncertain whether this results from a generally high gene frequency for the disorders or from consanguinity and other more local factors.This publication has 16 references indexed in Scilit:
- GENETIC DISORDERS IN GYPSIESThe Lancet, 1975
- GENETIC DISORDERS IN GYPSIESThe Lancet, 1975
- Screening for inherited metabolic disease in Wales using urine-impregnated filter paper.Archives of Disease in Childhood, 1975
- AnthropologicaI significance of phenylketonuriaClinical Genetics, 1975
- Gypsy isolates in SloveniaJournal of Biosocial Science, 1969
- Gypsy isolates in Slovenia.1969
- Hereditary Galactokinase Deficiency, a Newly Recognized Cause of Juvenile Cataracts31Pediatric Research, 1966
- The birthplaces of parents and grandparents of a series of patients with phenylketonuria in south-east EnglandAnnals of Human Genetics, 1961
- SPORADIC NON-ENDEMIC GOITROUS CRETINISM: HEREDITARY TRANSMISSIONThe Lancet, 1956
- The Dialect of the Gypsies of Wales being the Older Form of British Romani Preserved in the Speech of the Clan of Abram WoodThe Modern Language Review, 1927