Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome
Author:
Publisher
Wiley
Subject
Psychiatry and Mental health,Neurology (clinical),Neurology,Arts and Humanities (miscellaneous),Rehabilitation
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2788.1995.tb00576.x/fullpdf
Reference27 articles.
1. FMRi protein: conserved RNP family domains and selective RNA binding;Ashley;Science,1993
2. Fragile X syndrome: a major cause of X-linked mental retardation;Butler;Comprehensive Therapy,1988
3. Chromosome lesions which could be interpreted as ‘fragile sites’ on the distal end of Xq;Butler;American Journal Medical Genetics,1990
4. Anthropometric comparison of mentally retarded males with and without the fragile X syndrome;Butler;American Journal Medical Genetics,1991a
5. A 15 item checklist for screening mentally retarded males for the fragile X syndrome;Butler;Clinical Genetics,1991b
Cited by 3 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. FRAXA Screening in Brazilian Institutionalized Individuals with Nonspecific Severe Mental Retardation;Genetic Testing;2000-09
2. Screen for MAOA mutations in target human groups;American Journal of Medical Genetics;1999-02-05
3. Screening for Fragile X Syndrome: Information Needs for Health Planners;Journal of Medical Screening;1997-06
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