The inactivation of the fragile X chromosome in female carriers of the Martin Bell syndrome as studied by two different methods
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb03362.x/fullpdf
Reference14 articles.
1. Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin;Carpenter;Am. J. Dis. Child.,1982
2. Verification of Lyon's hypothesis in fragile X carriers;Arce;Hum. Genet.,1984
3. Inactivation pattern of the fragile X in heterozygous carriers;Fryns;Hum. Genet.,1984
4. Replication status of the fragile X chromosome, fra(X)(q27) in three heterozygous females;Howell;Hum. Genet.,1982
5. X-linked mental retardation: a study of seven families;Jacobs;Am. J. Med. Genet.,1980
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1. Cognitive and Visual Processing Skills and Their Relationship to Mutation Size in Full and Premutation Female Fragile X Carriers;Optometry and Vision Science;2000-11
2. Contribution of the FMR1 gene mutation to human intellectual dysfunction;Nature Genetics;1995-11
3. Molecular-neurobehavioral associations in females with the fragile X full mutation;American Journal of Medical Genetics;1994-07-15
4. Prenatal detection of Fra(X)(q27.3) in female identical twins: Reliability of low level cytogenetic prenatal expression in females;American Journal of Medical Genetics;1992-04-15
5. The fragile X Syndrome;Molecular Genetic Medicine;1992
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