| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/(SICI)1096-8628(19990402)83:4<237::AID-AJMG2>3.0.CO;2-8 |
| P2093 | author name string | C. Schwartz | |
| G. Neri | |||
| H. Lubs | |||
| L. Tranebjaerg | |||
| J. Arena | |||
| P. Chiurazzi | |||
| P433 | issue | 4 | |
| P1104 | number of pages | 11 | |
| P304 | page(s) | 237-247 | |
| P577 | publication date | 1999-04-02 | |
| P1433 | published in | American Journal of Medical Genetics Part A | Q15755121 |
| P1476 | title | XLMR genes: Update 1998 | |
| P478 | volume | 83 |
| Q48117476 | A comparative expression analysis of four MRX genes regulating intracellular signalling via small GTPases |
| Q28198461 | A novel deafness/dystonia peptide gene mutation that causes dystonia in female carriers of Mohr-Tranebjaerg syndrome |
| Q22011110 | A novel ribosomal S6-kinase (RSK4; RPS6KA6) is commonly deleted in patients with complex X-linked mental retardation |
| Q77976950 | Carpenter-Waziri syndrome results from a mutation in XNP |
| Q47826552 | Cloning of Z39Ig, a novel gene with immunoglobulin-like domains located on human chromosome X. |
| Q30572673 | Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one family |
| Q34306151 | In search of the MRX genes |
| Q51970341 | Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21. |
| Q51967079 | Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family. |
| Q51964852 | Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2. |
| Q51929767 | Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardation. |
| Q50312539 | MECP2 mutation in male patients with non-specific X-linked mental retardation. |
| Q48746278 | Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26. |
| Q51972756 | Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian family. |
| Q24290378 | Molecular characterization of a new human T-box gene (TBX22) located in xq21.1 encoding a protein containing a truncated T-domain |
| Q51972754 | Molecular study of the PAK3 and GDI1 genes in nonsyndromic X-linked mental retardation spanish patients. |
| Q24290357 | Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation |
| Q51972183 | Non-syndromic mental retardation segregating with an apparently balanced t(1;17) reciprocal translocation through three generations. |
| Q51963521 | Novel X-linked mental retardation syndrome with short stature maps to Xq24. |
| Q24538917 | Renpenning syndrome maps to Xp11. |
| Q40697551 | Sixty years of X-linked mental retardation: a historical footnote |
| Q34069962 | Syndromic XLMR genes (MRXS): update 2000. |
| Q34464659 | The X--a sexy chromosome |
| 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 |
| Q77976928 | The other side of the coin: a hypothesis concerning the importance of genes for high intelligence and evolution of the X chromosome |
| Q73013123 | X-linked mental retardation |
| Q51983448 | X-linked mental retardation syndrome with characteristic "coarse" facial appearance, brachydactyly, and short stature maps to proximal Xq. |
| Q48168814 | X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between xq21.33 and Xq23. |
| Q51983447 | X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28. |
| Q24563790 | X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28 |
| Q30579103 | X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region |
| Q35026980 | X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms |
| Q34265101 | X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome |
| Q51983452 | XLMR database. |
| Q34225912 | XLMR genes: update 2000. |
| Q34736415 | XLMR genes: update 2007. |
| Q74030851 | [Recent advances in the genetics and physiopathology of X chromosomal mental retardation] |
Search more.