| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/1096-8628(20001023)94:5<364::AID-AJMG3>3.0.CO;2-O |
| P698 | PubMed publication ID | 11050618 |
| P2093 | author name string | Chelly J | |
| P2860 | cites work | A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation | Q22009561 |
| Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation | Q24314619 | ||
| Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome | Q24336705 | ||
| PAK3 mutation in nonsyndromic X-linked mental retardation | Q28281729 | ||
| Membrane targeting of p21-activated kinase 1 (PAK1) induces neurite outgrowth from PC12 cells | Q28579492 | ||
| Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation | Q33724064 | ||
| A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation. | Q33888444 | ||
| Identification of the gene FMR2, associated with FRAXE mental retardation | Q34385889 | ||
| Mutations in GDI1 are responsible for X-linked non-specific mental retardation | Q34471146 | ||
| Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions | Q36759870 | ||
| Epidemiology of mental retardation--a Swedish survey. | Q39350924 | ||
| XLMR genes: update 1996. | Q41127106 | ||
| Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor. | Q47827573 | ||
| X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: the European XLMR consortium. | Q51983442 | ||
| Integrin associated proteins | Q77565695 | ||
| P433 | issue | 5 | |
| P304 | page(s) | 364-366 | |
| P577 | publication date | 2000-10-01 | |
| P1433 | published in | American Journal of Medical Genetics Part A | Q15755121 |
| P1476 | title | MRX review | |
| P478 | volume | 94 |
| Q51972762 | 9th international workshop on fragile X syndrome and X-linked mental retardation. |
| Q51953580 | Another family with nonspecific X-linked mental retardation (MRX78) maps to Xp11.4-p11.23. |
| Q38578790 | Genetic basis of cognitive disability |
| Q51946976 | Localization of a non-syndromic X-linked mental retardation gene (MRX80) to Xq22-q24. |
| Q24291714 | NXF5, a novel member of the nuclear RNA export factor family, is lost in a male patient with a syndromic form of mental retardation |
| Q35974513 | Rho proteins, mental retardation and the neurobiological basis of intelligence |
| Q33945296 | The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR). |
| Q34273185 | The human gene CXorf17 encodes a member of a novel family of putative transmembrane proteins: cDNA cloning and characterization of CXorf17 and its mouse ortholog orf34 |
| Q24535650 | The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation |
| Q34594213 | The role of Rho GTPases in disease development |
| Q36239035 | X linked mental retardation: a clinical guide |
| Q24563790 | X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28 |
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