Literature DB >> 7783162

FRAXE and mental retardation.

J C Mulley1, S Yu, D Z Loesch, D A Hay, A Donnelly, A K Gedeon, P Carbonell, I López, G Glover, I Gabarrón.   

Abstract

Mental impairment and instability of the CCG repeat at FRAXE is described in six kindreds. Cosegregation of FRAXA and FRAXE was found within one of these kindreds. Cytogenetic expression of FRAXE was shown to skip a generation when associated with a reduction in size of the CCG expansion when transmitted through a male; however, in general, transmission occurred through females and a copy number increased from one generation to the next. In these respects the behaviour of FRAXE paralleled that of FRAXA. A relationship between FRAXE and non-specific mental impairment is strongly suggested by the occurrence in these families of more mentally impaired male and female carriers, after removal of index cases, than could reasonably be expected by chance.

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Year:  1995        PMID: 7783162      PMCID: PMC1050310          DOI: 10.1136/jmg.32.3.162

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


  25 in total

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2.  Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicap.

Authors:  S J Knight; M A Voelckel; M C Hirst; A V Flannery; A Moncla; K E Davies
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

3.  The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.

Authors:  M C Hirst; A Barnicoat; G Flynn; Q Wang; M Daker; V J Buckle; K E Davies; M Bobrow
Journal:  Hum Mol Genet       Date:  1993-02       Impact factor: 6.150

4.  Genotype-phenotype relationships in fragile X syndrome: a family study.

Authors:  D Z Loesch; R Huggins; D A Hay; A K Gedeon; J C Mulley; G R Sutherland
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

5.  Heritable unstable DNA sequences and hypermethylation associated with fragile X syndrome in Japanese families.

Authors:  T Hori; M Yamauchi; N Seki; S Tsuji; I Kondo
Journal:  Clin Genet       Date:  1993-01       Impact factor: 4.438

6.  Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

Authors:  S J Knight; A V Flannery; M C Hirst; L Campbell; Z Christodoulou; S R Phelps; J Pointon; H R Middleton-Price; A Barnicoat; M E Pembrey
Journal:  Cell       Date:  1993-07-16       Impact factor: 41.582

7.  The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

Authors:  E Reyniers; L Vits; K De Boulle; B Van Roy; D Van Velzen; E de Graaff; A J Verkerk; H Z Jorens; J K Darby; B Oostra
Journal:  Nat Genet       Date:  1993-06       Impact factor: 38.330

8.  Somatic instability of CTG repeat in myotonic dystrophy.

Authors:  T Ashizawa; J R Dubel; Y Harati
Journal:  Neurology       Date:  1993-12       Impact factor: 9.910

9.  Segregation of the fragile X mutation from an affected male to his normal daughter.

Authors:  P J Willems; B Van Roy; K De Boulle; L Vits; E Reyniers; O Beck; J E Dumon; A Verkerk; B Oostra
Journal:  Hum Mol Genet       Date:  1992-10       Impact factor: 6.150

10.  Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy.

Authors:  M Anvret; G Ahlberg; U Grandell; B Hedberg; K Johnson; L Edström
Journal:  Hum Mol Genet       Date:  1993-09       Impact factor: 6.150

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  19 in total

Review 1.  Modifiers and mechanisms of multi-system polyglutamine neurodegenerative disorders: lessons from fly models.

Authors:  Moushami Mallik; Subhash C Lakhotia
Journal:  J Genet       Date:  2010-12       Impact factor: 1.166

2.  A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom.

Authors:  S J Knight; R J Ritchie; L Chakrabarti; G Cross; G R Taylor; R F Mueller; J Hurst; J Paterson; J R Yates; D J Dow; K E Davies
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

3.  Fragile X syndrome is less common than previously estimated.

Authors:  J E Morton; S Bundey; T P Webb; F MacDonald; P M Rindl; S Bullock
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

4.  The FRAXE Syndrome: is it time for routine screening?

Authors:  W T Brown
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

5.  Clinical, cytogenetic, and molecular analysis of three families with FRAXE.

Authors:  A J Barnicoat; Q Wang; J Turk; E Green; C G Mathew; G Flynn; V Buckle; M Hirst; K Davies; M Bobrow
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

6.  Fragile XE: an important differential diagnosis.

Authors:  Venkataraman Krishnan; Penny Clouston; Mark Crocker; James Macpherson; Frances Heydon; Helen Stewart
Journal:  BMJ Case Rep       Date:  2010-03-23

7.  FRAXA and FRAXE: the results of a five year survey.

Authors:  S A Youings; A Murray; N Dennis; S Ennis; C Lewis; N McKechnie; M Pound; A Sharrock; P Jacobs
Journal:  J Med Genet       Date:  2000-06       Impact factor: 6.318

8.  Genetic Counseling for Fragile X Syndrome: Recommendations of the National Society of Genetic Counselors.

Authors:  N McIntosh; L W Gane; A McConkie-Rosell; R L Bennett
Journal:  J Genet Couns       Date:  2000-08       Impact factor: 2.537

9.  Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring.

Authors:  D Z Loesch; R Huggins; V Petrovic; H Slater
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

10.  Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population.

Authors:  D C Crawford; K L Meadows; J L Newman; L F Taft; D L Pettay; L B Gold; S J Hersey; E F Hinkle; M L Stanfield; P Holmgreen; M Yeargin-Allsopp; C Boyle; S L Sherman
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

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