Literature DB >> 19460939

You can build it ... but will they come?: the potential "expansion" of testing methodologies for fragile X syndrome.

Nicholas T Potter1.   

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Year:  2009        PMID： 19460939      PMCID： PMC2710702          DOI： 10.2353/jmoldx.2009.090047

Source DB:  PubMed          Journal:  J Mol Diagn        ISSN： 1525-1578            Impact factor:   5.568


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  16 in total

1.  Actively acquired tolerance of foreign cells.

Authors:  R E BILLINGHAM; L BRENT; P B MEDAWAR
Journal:  Nature       Date:  1953-10-03       Impact factor: 49.962

2.  Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.

Authors:  I Oberlé; F Rousseau; D Heitz; C Kretz; D Devys; A Hanauer; J Boué; M F Bertheas; J L Mandel
Journal:  Science       Date:  1991-05-24       Impact factor: 47.728

3.  Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.

Authors:  E J Kremer; M Pritchard; M Lynch; S Yu; K Holman; E Baker; S T Warren; D Schlessinger; G R Sutherland; R I Richards
Journal:  Science       Date:  1991-06-21       Impact factor: 47.728

4.  An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 gene.

Authors:  Alessandro Saluto; Alessandro Brussino; Flora Tassone; Carlo Arduino; Claudia Cagnoli; Patrizia Pappi; Paul Hagerman; Nicola Migone; Alfredo Brusco
Journal:  J Mol Diagn       Date:  2005-11       Impact factor: 5.568

5.  Improved fluorescent PCR-based assay for sizing CGG repeats at the FRAXA locus.

Authors:  C Houdayer; A Lemonnier; M Gerard; C Chauve; M Tredano; T B de Villemeur; P Aymard; J P Bonnefont; D Feldmann
Journal:  Clin Chem Lab Med       Date:  1999-04       Impact factor: 3.694

6.  Automated Detection of Trinucleotide Repeats in Fragile X Syndrome.

Authors: 
Journal:  Mol Diagn       Date:  1997-12

7.  A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males.

Authors:  L A Haddad; R C Mingroni-Netto; A M Vianna-Morgante; S D Pena
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

8.  Prenatal diagnosis and carrier screening for fragile X by PCR.

Authors:  W T Brown; S Nolin; G Houck; X Ding; A Glicksman; S Y Li; S Stark-Houck; P Brophy; C Duncan; C Dobkin; E Jenkins
Journal:  Am J Med Genet       Date:  1996-07-12

9.  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

10.  Fragile X syndrome: diagnostic and carrier testing.

Authors:  Stephanie Sherman; Beth A Pletcher; Deborah A Driscoll
Journal:  Genet Med       Date:  2005-10       Impact factor: 8.822
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  1 in total

1.  The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge.

Authors:  François Rousseau; Yves Labelle; Johanne Bussières; Carmen Lindsay
Journal:  Clin Biochem Rev       Date:  2011-08
  1 in total

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