Literature DB >> 6693128

Inactivation pattern of the fragile X in heterozygous carriers.

J P Fryns, A Kleczkowska, E Kubień, P Petit, H Van den Berghe.   

Abstract

Chromosome analysis with conventional staining, G-banding, and R-banding with 5-bromodeoxyuridine (BrdU) incorporation were performed on the lymphocytes of ten females, who were heterozygous for the fragile X-chromosome. Mental development of these females varied greatly: moderate to severe mental retardation was found in one and moderate mental retardation in four females. Normal to borderline intelligence was found in three and normal intelligence was noted in two further females. The discrepancy in percentage of active fragile X-chromosomes in the five females with moderate mental retardation was found to be 60-100% (mean value: 80%). The three women with normal to borderline intelligence showed a corresponding discrepancy from 57 to 86% (mean value: 77%) of active fragile X-chromosomes. Finally, two female heterozygotes for fragile X with normal intelligence showed 70 and 76% (mean value 73%) of active fragile X-chromosomes. The phenotypic features also did not seem to correspond with the X-chromosome inactivation pattern. Based on the data obtained, we suggest that there is no evident correlation between the frequency of the active fragile X chromosomes and the mental status of these females.

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Year:  1984        PMID: 6693128     DOI: 10.1007/bf00291567

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  7 in total

1.  Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium.

Authors:  G R Sutherland
Journal:  Science       Date:  1977-07-15       Impact factor: 47.728

2.  Screening for fra(X)(q) in a population of mentally retarded males.

Authors:  U Froster-Iskenius; G Felsch; C Schirren; E Schwinger
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome.

Authors:  P A Jacobs; M Mayer; J Matsuura; F Rhoads; S C Yee
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  X-linked mental retardation: a study of 7 families.

Authors:  P A Jacobs; T W Glover; M Mayer; P Fox; J W Gerrard; H G Dunn; D S Herbst
Journal:  Am J Med Genet       Date:  1980

5.  Activity of the fragile X in heterozygous carriers.

Authors:  I A Uchida; E M Joyce
Journal:  Am J Hum Genet       Date:  1982-03       Impact factor: 11.025

Review 6.  Nonspecific X-linked mental retardation I: a review with information from 24 new families.

Authors:  D S Herbst
Journal:  Am J Med Genet       Date:  1980

7.  Late-replicating ring X-chromosomes identified by R-banding after BrdU pulse. Three new examples of mosaicism 45, XO/46, Xr(X).

Authors:  A Hagemeijer; J Hoovers; I Hasper-Voogt; T Von Ruhe-Zurcher; D Bootsma
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

  7 in total
  8 in total

1.  Replication patterns of the fragile X in heterozygous carriers: analysis by a BrdUrd antibody method.

Authors:  H Ohashi; A Kuwano; M Tsukahara; T Arinami; T Kajii
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

2.  Mental status of females with an FMR1 gene full mutation.

Authors:  B B de Vries; A M Wiegers; A P Smits; S Mohkamsing; H J Duivenvoorden; J P Fryns; L M Curfs; D J Halley; B A Oostra; A M van den Ouweland; M F Niermeijer
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

3.  Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect.

Authors:  M Rocchi; N Archidiacono; A Rinaldi; G Filippi; G Bartolucci; G S Fancello; M Siniscalco
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

4.  Fragile X syndrome: clinical, cytogenetic, biochemical and molecular features.

Authors:  J C Mixon; V G Dev
Journal:  Indian J Pediatr       Date:  1986 Jul-Aug       Impact factor: 1.967

5.  Replication status of fragile X(q27.3) in 13 female heterozygotes.

Authors:  E Tuckerman; T Webb; A Thake
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

6.  Verification of Lyon's hypothesis in fragile X carriers.

Authors:  M A De Arce
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Fragile Xq27.3 in female heterozygotes for the Martin-Bell syndrome.

Authors:  T Webb; P A Jacobs
Journal:  J Med Genet       Date:  1990-10       Impact factor: 6.318

8.  A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.

Authors:  F Rousseau; D Heitz; J Tarleton; J MacPherson; H Malmgren; N Dahl; A Barnicoat; C Mathew; E Mornet; I Tejada
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

  8 in total

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