Verification of Lyon's hypothesis in fragile X carriers
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00292599.pdf
Reference6 articles.
1. Fryns JP, Kleczkowska A, Kubien E, Petit P, Van den Berghe H (1984) Inactivation pattern of the fragile X in heterozygous carriers. Hum Genet 65:400?402
2. Howell RT, McDermott A (1982) Replication status of the fragile X chromosome, fra(X)(q27), in three heterozygous females. Hum Genet 62:282?284
3. Paul J, Froster-Iskenius U, Moje W, Schwinger E (1984) Heterozygous female carriers of the marker-X-chromosome: IQ estimation and replication status of fra(X)(q). Hum Genet 66:344?347
4. Sherman SL, Morton NE, Jacobs PA, Turner G (1984) The marker (X) syndrome: a cytogenetic and genetic analysis. Ann Hum Genet 48:21?37
5. Uchida IA, Joyce EM (1982) Activity of the fragile X in heterozygous carriers. Am J Hum Genet 34:286?293
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1. Fragile X leads to X chromosome loss: Comments from a cytogeneticist;American Journal of Medical Genetics Part A;2010-06-25
2. The inactivation of the fragile X chromosome in female carriers of the Martin Bell syndrome as studied by two different methods;Clinical Genetics;2008-06-28
3. Screening for Fragile X Syndrome: Information Needs for Health Planners;Journal of Medical Screening;1997-06
4. Effect of X inactivation on fragile X frequency and mental retardation;American Journal of Medical Genetics;1991-02-01
5. Fra(X) frequency on the active X-chromosome and phenotype in heterozygous carriers of the fra(X) form of mental retardation;American Journal of Medical Genetics;1988-05
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