Literature DB >> 1681307

Prenatal diagnosis of fragile X syndrome.

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Year:  1991        PMID： 1681307

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  5 in total

1.  Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.

Authors:  G A Flynn; M C Hirst; S J Knight; J N Macpherson; J C Barber; A V Flannery; K E Davies; V J Buckle
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

2.  Prenatal diagnosis of a hypermethylated full fragile X mutation in chorionic villi of a male fetus.

Authors:  K Suzumori; M Yamauchi; N Seki; I Kondo; T Hori
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

3.  Experience with direct molecular diagnosis of fragile X.

Authors:  J C Mulley; S Yu; A K Gedeon; A Donnelly; G Turner; D Loesch; C J Chapman; R J Gardner; R I Richards; G R Sutherland
Journal:  J Med Genet       Date:  1992-06       Impact factor: 6.318

4.  Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation.

Authors:  B A Oostra; P B Jacky; W T Brown; F Rousseau
Journal:  J Med Genet       Date:  1993-05       Impact factor: 6.318

5.  DNA testing for fragile X syndrome in schools for learning difficulties.

Authors:  S F Slaney; A O Wilkie; M C Hirst; R Charlton; M McKinley; J Pointon; Z Christodoulou; S M Huson; K E Davies
Journal:  Arch Dis Child       Date:  1995-01       Impact factor: 3.791
  5 in total

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