Literature DB >> 1605211

Study of individuals possibly affected with the fragile X syndrome in a large Swedish family in the 18th to 20th centuries.

U Drugge, G Holmgren, H K Blomquist, N Dahl, K H Gustavson, H Malmgren.   

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Year:  1992        PMID： 1605211     DOI： 10.1002/ajmg.1320430154

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  3 in total

1.  Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes.

Authors:  C Oudet; E Mornet; J L Serre; F Thomas; S Lentes-Zengerling; C Kretz; C Deluchat; I Tejada; J Boué; A Boué
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

2.  Origins of the fragile X syndrome mutation.

Authors:  M C Hirst; S J Knight; Z Christodoulou; P K Grewal; J P Fryns; K E Davies
Journal:  J Med Genet       Date:  1993-08       Impact factor: 6.318

Review 3.  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
  3 in total

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