Literature DB >> 8644726

Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution.

W T Brown, N Zhong, C Dobkin.   

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Year:  1996        PMID： 8644726      PMCID： PMC1914571     

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


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  11 in total

1.  Microsatellite evolution--evidence for directionality and variation in rate between species.

Authors:  D C Rubinsztein; W Amos; J Leggo; S Goodburn; S Jain; S H Li; R L Margolis; C A Ross; M A Ferguson-Smith
Journal:  Nat Genet       Date:  1995-07       Impact factor: 38.330

2.  Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate.

Authors:  T Arinami; M Asano; K Kobayashi; H Yanagi; H Hamaguchi
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132

Review 3.  Linkage disequilibrium as a gene-mapping tool.

Authors:  L B Jorde
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

4.  Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation.

Authors:  J N Macpherson; H Bullman; S A Youings; P A Jacobs
Journal:  Hum Mol Genet       Date:  1994-03       Impact factor: 6.150

5.  Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.

Authors:  N Zhong; X Liu; S Gou; G E Houck; S Li; C Dobkin; W T Brown
Journal:  Am J Med Genet       Date:  1994-07-15

6.  Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene.

Authors:  S D Pena; K T de Souza; M de Andrade; R Chakraborty
Journal:  Proc Natl Acad Sci U S A       Date:  1994-01-18       Impact factor: 11.205

7.  Fragile X founder chromosome effects: linkage disequilibrium or microsatellite heterogeneity?

Authors:  N Zhong; L Ye; C Dobkin; W T Brown
Journal:  Am J Med Genet       Date:  1994-07-15

8.  Evidence of founder chromosomes in fragile X syndrome.

Authors:  R I Richards; K Holman; K Friend; E Kremer; D Hillen; A Staples; W T Brown; P Goonewardena; J Tarleton; C Schwartz
Journal:  Nat Genet       Date:  1992-07       Impact factor: 38.330

9.  Fragile X gene instability: anchoring AGGs and linked microsatellites.

Authors:  N Zhong; W Yang; C Dobkin; W T Brown
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

10.  Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer.

Authors:  N de Wind; M Dekker; A Berns; M Radman; H te Riele
Journal:  Cell       Date:  1995-07-28       Impact factor: 41.582
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  2 in total

1.  Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.

Authors:  D C Crawford; C E Schwartz; K L Meadows; J L Newman; L F Taft; C Gunter; W T Brown; N J Carpenter; P N Howard-Peebles; K G Monaghan; S L Nolin; A L Reiss; G L Feldman; E M Rohlfs; S T Warren; S L Sherman
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

2.  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
  2 in total

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