| scholarly article | Q13442814 |
| P356 | DOI | 10.1177/088307389801300507 |
| P698 | PubMed publication ID | 9620015 |
| P2093 | author name string | L S Dure | |
| A K Percy | |||
| T W Kurczynski | |||
| D Brunelle | |||
| M M Woodcock | |||
| N C Schanen | |||
| P2860 | cites work | A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map. | Q35249570 |
| Genetic aspects of Rett syndrome | Q39545733 | ||
| P433 | issue | 5 | |
| P921 | main subject | Rett syndrome | Q917357 |
| neonatal hypoxic-ischemic encephalopathy | Q5832339 | ||
| P304 | page(s) | 229-231 | |
| P577 | publication date | 1998-05-01 | |
| P1433 | published in | Journal of Child Neurology | Q6294935 |
| P1476 | title | Neonatal encephalopathy in two boys in families with recurrent Rett syndrome | |
| P478 | volume | 13 |
| Q37216254 | A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome |
| Q30381238 | Characterization of Rett Syndrome-like phenotypes in Mecp2-knockout rats |
| Q29616328 | Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice |
| Q50791963 | Distinct de novo deletions in a brother-sister pair with RTT: a case report. |
| Q36286566 | Does genotype predict phenotype in Rett syndrome? |
| Q33835767 | Familial cases and male cases with MECP2 mutations |
| Q30607592 | Family data in Rett syndrome: association with other genetic disorders |
| Q48693103 | Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems |
| Q39126183 | Functional assessment of MeCP2 in Rett syndrome and cancers of breast, colon, and prostate |
| Q34733498 | Genetic basis of Rett syndrome |
| Q34542327 | Genetic effects on human cognition: lessons from the study of mental retardation syndromes |
| Q40268539 | Identifying patterns of communicative behaviors in girls with Rett syndrome |
| Q35838075 | Linking epigenetics to human disease and Rett syndrome: the emerging novel and challenging concepts in MeCP2 research |
| Q35436994 | MECP2 mutation in non-fatal, non-progressive encephalopathy in a male |
| Q34733505 | MeCP2 and other methyl-CpG binding proteins |
| Q37632847 | MeCP2-Related Diseases and Animal Models |
| Q38821957 | MeCP2-regulated miRNAs control early human neurogenesis through differential effects on ERK and AKT signaling |
| Q77220748 | Metacarpophalangeal pattern profile and bone age in Rett syndrome: further radiological clues to the diagnosis |
| Q51872632 | Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation. |
| Q41212293 | Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys |
| Q33805791 | Molecular approaches to the Rett syndrome gene |
| Q24534159 | Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation |
| Q28180155 | Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2) |
| Q48856336 | Occurrence of Rett syndrome in boys |
| Q46355799 | Patterns of pregnancy loss, perinatal mortality, and postneonatal childhood deaths in families of girls with Rett syndrome. |
| Q48296618 | Progressive cerebellar degenerative changes in the severe mental retardation syndrome caused by duplication of MECP2 and adjacent loci on Xq28. |
| Q34460580 | Rethinking the fate of males with mutations in the gene that causes Rett syndrome |
| Q24616417 | Rett syndrome and MeCP2: linking epigenetics and neuronal function |
| Q34146268 | Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots |
| Q35077740 | Rett syndrome. Current status and new vistas |
| Q34460607 | Rett syndrome: clinical correlates of the newly discovered gene |
| Q48650852 | Rett syndrome: clinical manifestations in males with MECP2 mutations |
| Q28088283 | Rett syndrome: disruption of epigenetic control of postnatal neurological functions |
| Q36908704 | Rett syndrome: exploring the autism link |
| Q34141668 | Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations |
| Q30639662 | Rett syndrome: review of biological abnormalities. |
| Q38950303 | Social-emotional instability in individuals with Rett syndrome: parents' experiences with second stage behaviour |
| Q34733514 | The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome |
| Q33762214 | The role of MeCP2 in brain development and neurodevelopmental disorders |
| Q34387585 | Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain |
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