In search of the MRX genes
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference47 articles.
1. PAK3 mutation in nonsyndromic X-linked mental retardation
2. Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor
3. Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation
4. IRAK: A Kinase Associated with the Interleukin-1 Receptor
5. A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation
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1. Pattern of cytogenetic abnormalities in syndromic mental retardation/intellectual disability in Kashmir region of Jammu and Kashmir;Gene Reports;2021-09
2. Chromosomal Abnormalities in Patients with Intellectual Disability: A 21-Year Retrospective Study;Human Heredity;2018
3. Clinical checklists in the selection of mentally retarded males for molecular screening of fragile X syndrome;Genetics and Molecular Biology;2007
4. Partial tandem duplication ofGRIA3 in a male with mental retardation;American Journal of Medical Genetics Part A;2007
5. Fine mapping and clinical reevaluation of a Brazilian pedigree with a severe form of X-linked mental retardation associated with other neurological dysfunction;American Journal of Medical Genetics Part A;2004-03-05
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