Literature DB >> 6731439

Fragile (X) X-linked mental retardation. II. Frequency and replication pattern of fragile (X)(q28) in heterozygotes.

J H Knoll, A E Chudley, J W Gerrard.   

Abstract

The frequency of cytologic expression and the replication pattern of the fragile (X) [fra(X)] were investigated in 28 fra(X) heterozygotes, of which 25 agreed to psychological assessment. One-third of the heterozygotes in this study are mentally retarded. The intellectually impaired carriers had a higher frequency of fra(X) and a higher proportion of early-replicating fra(X) than the normally intelligent carriers. The early-replicating fra(X) accounted for 39% of the variability in IQ and the late-replicating fra(X) for 12%. Age had a minimal inverse effect on fra(X) expression and replication pattern. Thus, it appears that mental retardation in females heterozygous for the fra(X) may largely be a function of the proportion of cells with an early-replicating, active X chromosome possessing the fragile site.

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Year:  1984        PMID: 6731439      PMCID: PMC1684461     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  17 in total

1.  Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy.

Authors:  H F Willard; S A Latt
Journal:  Am J Hum Genet       Date:  1976-05       Impact factor: 11.025

2.  Recessive sex-linked mental retardation in the absence of other recognizable abnormalities. Report of a family.

Authors:  R D Snyder; A Robinson
Journal:  Clin Pediatr (Phila)       Date:  1969-11       Impact factor: 1.168

3.  X-linked mental deficiency megalotestes syndrome.

Authors:  R H Ruvalcaba; S A Myhre; E C Roosen-Runge; J B Beckwith
Journal:  JAMA       Date:  1977-10-10       Impact factor: 56.272

4.  X-linked recessively inherited non-specific mental retardation. Report of a large family.

Authors:  J Deroover; J P Fryns; C Parloir; H Van den Berghe
Journal:  Ann Genet       Date:  1977-12

5.  Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).

Authors:  M Jennings; J G Hall; H Hoehn
Journal:  Am J Med Genet       Date:  1980

6.  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

7.  X-linked mental retardation, macro-orchidism, and the Xq27 fragile site.

Authors:  G Turner; A Daniel; M Frost
Journal:  J Pediatr       Date:  1980-05       Impact factor: 4.406

8.  X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.

Authors:  K B Nielsen; N Tommerup; H Poulsen; M Mikkelsen
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of X-linked mental retardation.

Authors:  P N Howard-Peebles
Journal:  Am J Med Genet       Date:  1980

10.  Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

Authors:  G Turner; R Brookwell; A Daniel; M Selikowitz; M Zilibowitz
Journal:  N Engl J Med       Date:  1980-09-18       Impact factor: 91.245

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  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.  Parental inheritance and psychological disability in fragile X females.

Authors:  A L Reiss; L Freund; S Vinogradov; R Hagerman; A Cronister
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

3.  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

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.  Xq27 fragile site and hydrocephaly.

Authors:  E Tajara; M Varella-Garcia
Journal:  Am J Hum Genet       Date:  1985-11       Impact factor: 11.025

6.  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

7.  Frequency of the fragile X syndrome in institutionalized mentally retarded females in Japan.

Authors:  T Arinami; I Kondo; S Nakajima; H Hamaguchi
Journal:  Hum Genet       Date:  1987-08       Impact factor: 4.132

8.  Proteomics analysis identifies phosphorylation-dependent alpha-synuclein protein interactions.

Authors:  Melinda A McFarland; Christopher E Ellis; Sanford P Markey; Robert L Nussbaum
Journal:  Mol Cell Proteomics       Date:  2008-07-09       Impact factor: 5.911

  8 in total

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