Study of individuals possibly affected with the fragile X syndrome in a large swedish family in the 18th to 20th centuries-Reference-Cited by-同舟云学术

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

Published:1992-04-15 Issue:1-2 Volume:43 Page:353-354
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Drugge Ulf,Holmgren GöSta,Blomquist Hans Kison,Dahl Niklas,Gustavson Karl-Henrik,Malmgren Helena

Publisher

Wiley

Subject

Genetics (clinical)

Reference3 articles.

1. Fragile X families in a Northern Swedish County: A genealogical study of possibly affected individuals in the nineteenth century

2. Fragile X families in a Northern Swedish county - a genealogical study demonstrating apparent paternal transmission from the 18th century

3. Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The fragile X syndrome.;Journal of Medical Genetics;1998-07-01

2. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome;Human Molecular Genetics;1996-03-01

3. The fragile X mutation;Mental Retardation and Developmental Disabilities Research Reviews;1995

4. Population genetics of fragile X: A multiple allele model with variable risk of CGG repeat expansion;American Journal of Medical Genetics;1994-07-15

5. Origins of the fragile X syndrome mutation.;Journal of Medical Genetics;1993-08-01

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