Literature DB >> 7485183

The high prevalence of fragile X premutation carrier females: is this frequency unique to the French Canadian population?

S L Sherman.   

Abstract

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Year:  1995        PMID： 7485183      PMCID： PMC1801365     

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


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  18 in total

1.  An n-allele model for progressive amplification in the FMR1 locus.

Authors:  A Morris; N E Morton; A Collins; J Macpherson; D Nelson; S Sherman
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-23       Impact factor: 11.205

2.  Precursor arrays for triplet repeat expansion at the fragile X locus.

Authors:  M C Hirst; P K Grewal; K E Davies
Journal:  Hum Mol Genet       Date:  1994-09       Impact factor: 6.150

3.  Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.

Authors:  K Snow; D J Tester; K E Kruckeberg; D J Schaid; S N Thibodeau
Journal:  Hum Mol Genet       Date:  1994-09       Impact factor: 6.150

4.  Length of uninterrupted CGG repeats determines instability in the FMR1 gene.

Authors:  E E Eichler; J J Holden; B W Popovich; A L Reiss; K Snow; S N Thibodeau; C S Richards; P A Ward; D L Nelson
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

5.  Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

Authors:  A J Verkerk; M Pieretti; J S Sutcliffe; Y H Fu; D P Kuhl; A Pizzuti; O Reiner; S Richards; M F Victoria; F P Zhang
Journal:  Cell       Date:  1991-05-31       Impact factor: 41.582

6.  Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.

Authors:  Y H Fu; D P Kuhl; A Pizzuti; M Pieretti; J S Sutcliffe; S Richards; A J Verkerk; J J Holden; R G Fenwick; S T Warren
Journal:  Cell       Date:  1991-12-20       Impact factor: 41.582

7.  Variability of the genetic contribution of Quebec population founders associated to some deleterious genes.

Authors:  E Heyer; M Tremblay
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025

8.  Striking founder effect for the fragile X syndrome in Finland.

Authors:  C Oudet; H von Koskull; A M Nordström; M Peippo; J L Mandel
Journal:  Eur J Hum Genet       Date:  1993       Impact factor: 4.246

9.  Absence of expression of the FMR-1 gene in fragile X syndrome.

Authors:  M Pieretti; F P Zhang; Y H Fu; S T Warren; B A Oostra; C T Caskey; D L Nelson
Journal:  Cell       Date:  1991-08-23       Impact factor: 41.582

10.  Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

Authors:  F Rousseau; P Rouillard; M L Morel; E W Khandjian; K Morgan
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025
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  2 in total

1.  Fragile X premutations are not a major cause of early menopause.

Authors:  A Kenneson; D W Cramer; S T Warren
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

Review 2.  The fragile X syndrome.

Authors:  B B de Vries; D J Halley; B A Oostra; M F Niermeijer
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318
  2 in total

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