A non-syndromal form of X-linked mental retardation (XLMR) is linked toDXS14
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference9 articles.
1. LINKAGE ANALYSIS OF X-LINKED MENTAL RETARDATION WITH AND WITHOUT FRAGILE-X USING FACTOR IX GENE PROBE
2. Report of the committee on methods of linkage analysis and reporting
3. Nonspecific X-linked mental retardation II: The frequency in British Columbia
4. Colchester revisited: a genetic study of mental defect.
5. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14
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4. Diagnostic Exome Sequencing Identifies Two Novel IQSEC2 Mutations Associated with X-Linked Intellectual Disability with Seizures: Implications for Genetic Counseling and Clinical Diagnosis;Journal of Genetic Counseling;2013-12-04
5. Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability;European Journal of Human Genetics;2013-05-15
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