Literature DB >> 881706

Genetic study of Welsh gypsies.

E M Williams, P R Harper.   

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.

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Year:  1977        PMID： 881706      PMCID： PMC1013551          DOI： 10.1136/jmg.14.3.172

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  11 in total

1.  [A patient with kinky hair disease (Menke's disease)].

Authors:  J J Van de Kamp; H Oving; M A Giesbets
Journal:  Ned Tijdschr Geneeskd       Date:  1975-03-29

2.  [Occurrence of phenylketonuria in Bohemia & Moravia].

Authors:  J BLEHOVA; J DANESOVA; L GREC; F HAJEK; M MATOUSEK; V VOJTIK
Journal:  Cesk Pediatr       Date:  1959-06-05

3.  The birthplaces of parents and grandparents of a series of patients with phenylketonuria in in south-east England.

Authors:  C O CARTER; L I WOOLF
Journal:  Ann Hum Genet       Date:  1961-05       Impact factor: 1.670

4.  Sporadic non-endemic goitrous cretinism; hereditary transmission.

Authors:  J H HUTCHISON; E M MCGIRR
Journal:  Lancet       Date:  1956-06-30       Impact factor: 79.321

5.  Screening for inherited metabolic disease in Wales using urine-impregnated filter paper.

Authors:  D M Bradley
Journal:  Arch Dis Child       Date:  1975-04       Impact factor: 3.791

6.  Gypsy isolates in Slovenia.

Authors:  M Avcin
Journal:  J Biosoc Sci       Date:  1969-07

7.  Hypergalactosemia and galactosuria due to galactokinase deficiency in a newborn.

Authors:  O Thalhammer; R Gitzelmann; M Pantlitschko
Journal:  Pediatrics       Date:  1968-09       Impact factor: 7.124

8.  Letter: Genetic disorders in gypsies.

Authors:  E Passarge
Journal:  Lancet       Date:  1975-05-31       Impact factor: 79.321

9.  Letter: Genetic disorders in gypsies.

Authors:  P S Harper; E M Williams
Journal:  Lancet       Date:  1975-05-03       Impact factor: 79.321

10.  Genetic variation in Wales.

Authors:  P S Harper
Journal:  J R Coll Physicians Lond       Date:  1976-07
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  4 in total

1.  Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma.

Authors:  M Plásilová; I Stoilov; M Sarfarazi; L Kádasi; E Feráková; V Ferák
Journal:  J Med Genet       Date:  1999-04       Impact factor: 6.318

2.  Prevalence of congenital anomaly syndromes in a Spanish gypsy population.

Authors:  M L Martínez-Frías; E Bermejo
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

3.  Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of Wales.

Authors:  L A Tyfield; A L Meredith; M J Osborn; P S Harper
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

Review 4.  Traveller gypsies and primary care.

Authors:  G Feder
Journal:  J R Coll Gen Pract       Date:  1989-10
  4 in total

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