Literature DB >> 3688020

Sister chromatid exchange analysis in the Prader-Labhart-Willi syndrome.

M G Butler1, B B Jenkins.   

Abstract

The number of sister chromatid exchanges (SCE) and cell kinetics in lymphocytes were investigated from 16 Prader-Labhart-Willi syndrome (PLWS) patients [8 with 15q12 deletion (4 females, 4 males; mean age = 12.9y with age range of 0.3 to 24y), and 8 non-deletion (2 females, 6 males; means age = 16.8y with age range of 5 to 26y)], 18 parents of PLWS patients and age-matched control individuals. The average SCE frequency and standard deviation in PLWS patients with and without the chromosome 15 deletion was 6.6 +/- 1.3 and 6.2 +/- 0.8, respectively. Therefore no significant difference in SCE frequency or replicative index was found between the two PLWS subgroups. There was also no significant difference in SCE frequency or replicative index between the 16 PLWS patients and age-matched control subjects. The average SCE frequency and standard deviation in 8 fathers who were previously identified to have donated the chromosome 15 with the deletion in the child was 7.5 +/- 1.2, which was not significantly different from 8.5 +/- 2.0 seen in age-matched control subjects. There was also no significant difference in the SCE frequency or replicative index of 18 parents of PLWS patients with and without the chromosome 15 deletion when compared with age-matched control subjects.

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Mesh:

Year:  1987        PMID: 3688020      PMCID: PMC6684340          DOI: 10.1002/ajmg.1320280406

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  5 in total

1.  Analysis of chromosome breakage in the Prader-Labhart-Willi syndrome.

Authors:  M G Butler; B B Jenkins
Journal:  Am J Med Genet       Date:  1989-04

2.  Chromosome fragile sites in mentally retarded males: increased incidence with seizures and diphenylhydantoin therapy.

Authors:  K B Hodges; R S Larson; M G Butler
Journal:  Ann Clin Lab Sci       Date:  1998 Sep-Oct       Impact factor: 1.256

3.  Sister chromatid exchange analysis of the 15q11 region in Prader-Willi syndrome patients.

Authors:  S L Wenger; S D Rauch; J M Hanchett
Journal:  Hum Genet       Date:  1989-09       Impact factor: 4.132

4.  Bloom syndrome and maternal uniparental disomy for chromosome 15.

Authors:  T Woodage; M Prasad; J W Dixon; R E Selby; D R Romain; L M Columbano-Green; D Graham; P K Rogan; J R Seip; A Smith
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

5.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03
  5 in total

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