| P50 | author | Elke Holinski-Feder | Q43376219 |
| | Jozef Gécz | Q16230617 |
| | Frank Kooy | Q37843120 |
| P2093 | author name string | Charles Schwartz | |
| | Marc J Abramowicz | |
| | Daniel Christophe | |
| | Christiane Christophe-Hobertus | |
| P2860 | cites work | Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening? | Q44153653 |
| | Family MRX9 revisited: further evidence for locus heterogeneity in MRX. | Q51953231 |
| | Pericentromeric genes for non-specific X-linked mental retardation (MRX) | Q57971944 |
| | Identification of the gene encoding Brain Cell Membrane Protein 1 (BCMP1), a putative four-transmembrane protein distantly related to the Peripheral Myelin Protein 22 / Epithelial Membrane Proteins and the Claudins | Q21266638 |
| | A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58 | Q24679280 |
| | The cell junction protein VAB-9 regulates adhesion and epidermal morphology in C. elegans | Q30805771 |
| | A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation. | Q33888444 |
| | Novel mental retardation-epilepsy syndrome linked to Xp21.1-p11.4. | Q34108701 |
| | A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11. | Q34145980 |
| | Nonsyndromic X-linked mental retardation: where are the missing mutations? | Q34205119 |
| | XLMR genes: update 2000. | Q34225912 |
| | Monogenic causes of X-linked mental retardation. | Q34354315 |
| | Localization of non-specific X-linked mental retardation genes | Q42063982 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 22 | |
| P577 | publication date | 2004-09-02 | |
| P1433 | published in | BMC Medical Genetics | Q15759918 |
| P1476 | title | TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation | |
| P478 | volume | 5 | |